Are you over 18 and want to see adult content?
More Annotations
A complete backup of insurancebrokerageamerica.com
Are you over 18 and want to see adult content?
A complete backup of lojasrenner.com.br
Are you over 18 and want to see adult content?
A complete backup of simplelionheartlife.com
Are you over 18 and want to see adult content?
Favourite Annotations
A complete backup of https://jarurestaurant.weebly.com/
Are you over 18 and want to see adult content?
A complete backup of https://www.comandotorrent.tv/tag/gordo-torrents/
Are you over 18 and want to see adult content?
A complete backup of https://matkaindia.net/
Are you over 18 and want to see adult content?
A complete backup of https://iauashkezar.ac.ir/fa/
Are you over 18 and want to see adult content?
A complete backup of https://iwantclips.com/store/85792/Goddess-April
Are you over 18 and want to see adult content?
A complete backup of https://sattabossmatka.com/
Are you over 18 and want to see adult content?
A complete backup of https://dramasq.com/im-home/
Are you over 18 and want to see adult content?
Text
sensitivity.
IN-CELL WESTERN™
In-Cell Western™ is a simple and cost effective means for quantification of intracellular signaling in whole cells. This assay involves seeding cells in microtiter plates followed by fixation/permeabilization and subsequent labeling with activation state-specific or control antibodies, infrared-conjugated secondary antibodies, and/or far-red DNA dye. PHOSPHO-SRC FAMILY (TYR416) (D49G4) RABBIT MAB Phospho-Src Family (Tyr416) (D49G4) Rabbit mAb detects endogenous levels of Src only when phosphorylated at Tyr416. The antibody may cross-react with other Src family members (Lyn, Fyn, Lck, Yes and Hck) when phosphorylated at equivalent sites. It may cross react with overexpressed phosphorylated RTKs. NANOG (D73G4) XP® RABBIT MAB Wash sections in wash buffer for 5 min. Block each section with 100–400 µl of preferred blocking solution for 1 hr at room temperature. Remove blocking solution and add 100–400 µl primary antibody diluted in SignalStain ® Antibody Diluent ( #8112) to each section. Incubate overnight at 4°C. STAT1 (D1K9Y) RABBIT MAB IF. F. ChIP. Western blot analysis of extracts from A549 cells (lane 1) or STAT1 knock-out cells (lane 2) using Stat1 (D1K9Y) Rabbit mAb #14994 (upper), and β-actin (D6A8) Rabbit mAb #8457 (lower). The absence of signal in the STAT1 knock-out A549 cells confirms specificity of the antibody for STAT1. FOXP3 (D6O8R) RABBIT MAB FoxP3 (D6O8R) Rabbit mAb recognizes endogenous levels of total FoxP3 protein. This antibody recognizes mouse FoxP3 protein and is also reactive with human FoxP3; however, this antibody is not suggested for immunohistochemical analysis of human tissues. Instead, FoxP3 (D2W8E™) Rabbit mAb (IHC Specific) #98377 is recommended for IHCanalysis of
PYRUVATE DEHYDROGENASE (C54G1) RABBIT MAB In mammalian cells, the pyruvate dehydrogenase complex is located in the mitochondrial matrix (1). This complex is comprised of three enzymes: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2) and dihydrolipoamide dehydrogenase (E3). Pyruvate dehydrogenase (E1) consists of two subunits: α and β. PHOSPHO-MYOSIN IIA (SER1943) ANTIBODY The antibody was pre-incubated with peptides corresponding to unphosphorylated Myosin IIa or Myosin IIa phosphorylated at Ser1943, as indicated. Western blot analysis of extracts from HeLa, A-431 and 293T cells, untreated or treated with λ phosphatase and calf intestinal phosphatase (CIP), using Phospho-Myosin IIa (Ser1943)Antibody (upper) or
POLY/MONO-ADP RIBOSE (E6F6A) RABBIT MAB Western blot analysis of Colo 205 cells treated (+) with combinations of the following treatments as indicated: hydrogen peroxide (500 μM, 5 min), hydrogen peroxide-treated lysates treated with phosphodiesterase 1 (0.5 μg/mL, 4 hr at 37ºC), or with tcPARG (5 μM, 4 hr at 37ºC ) using Poly/Mono-ADP Ribose (E6F6A) Rabbit mAb (upper), or GAPDH (D16H11) XP ® Rabbit mAb #5174 (lower). ANTI-MOUSE IGG (H+L), F(AB')2 FRAGMENT (ALEXA FLUOR® 555 Anti-Mouse IgG (H+L) F (ab') 2 Fragment was conjugated to Alexa Fluor 555 fluorescent dye under optimal conditions and formulated at 2 mg/ml. This F (ab') 2 fragment product results in less non-specific binding, as it lacks the Fc domain that can bind to the cells with Fcreceptors.
CELL SIGNALING TECHNOLOGY (CST): ANTIBODIES, REAGENTSPRODUCTSSERVICESRESEARCHPROTEOMICSNEW AT CSTABOUT US An antibody shouldn’t be one of the variables in your experiment. Find out why customers rank CST highest for antibody specificity andsensitivity.
IN-CELL WESTERN™
In-Cell Western™ is a simple and cost effective means for quantification of intracellular signaling in whole cells. This assay involves seeding cells in microtiter plates followed by fixation/permeabilization and subsequent labeling with activation state-specific or control antibodies, infrared-conjugated secondary antibodies, and/or far-red DNA dye. PHOSPHO-SRC FAMILY (TYR416) (D49G4) RABBIT MAB Phospho-Src Family (Tyr416) (D49G4) Rabbit mAb detects endogenous levels of Src only when phosphorylated at Tyr416. The antibody may cross-react with other Src family members (Lyn, Fyn, Lck, Yes and Hck) when phosphorylated at equivalent sites. It may cross react with overexpressed phosphorylated RTKs. NANOG (D73G4) XP® RABBIT MAB Wash sections in wash buffer for 5 min. Block each section with 100–400 µl of preferred blocking solution for 1 hr at room temperature. Remove blocking solution and add 100–400 µl primary antibody diluted in SignalStain ® Antibody Diluent ( #8112) to each section. Incubate overnight at 4°C. STAT1 (D1K9Y) RABBIT MAB IF. F. ChIP. Western blot analysis of extracts from A549 cells (lane 1) or STAT1 knock-out cells (lane 2) using Stat1 (D1K9Y) Rabbit mAb #14994 (upper), and β-actin (D6A8) Rabbit mAb #8457 (lower). The absence of signal in the STAT1 knock-out A549 cells confirms specificity of the antibody for STAT1. FOXP3 (D6O8R) RABBIT MAB FoxP3 (D6O8R) Rabbit mAb recognizes endogenous levels of total FoxP3 protein. This antibody recognizes mouse FoxP3 protein and is also reactive with human FoxP3; however, this antibody is not suggested for immunohistochemical analysis of human tissues. Instead, FoxP3 (D2W8E™) Rabbit mAb (IHC Specific) #98377 is recommended for IHCanalysis of
PYRUVATE DEHYDROGENASE (C54G1) RABBIT MAB In mammalian cells, the pyruvate dehydrogenase complex is located in the mitochondrial matrix (1). This complex is comprised of three enzymes: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2) and dihydrolipoamide dehydrogenase (E3). Pyruvate dehydrogenase (E1) consists of two subunits: α and β. PHOSPHO-MYOSIN IIA (SER1943) ANTIBODY The antibody was pre-incubated with peptides corresponding to unphosphorylated Myosin IIa or Myosin IIa phosphorylated at Ser1943, as indicated. Western blot analysis of extracts from HeLa, A-431 and 293T cells, untreated or treated with λ phosphatase and calf intestinal phosphatase (CIP), using Phospho-Myosin IIa (Ser1943)Antibody (upper) or
POLY/MONO-ADP RIBOSE (E6F6A) RABBIT MAB Western blot analysis of Colo 205 cells treated (+) with combinations of the following treatments as indicated: hydrogen peroxide (500 μM, 5 min), hydrogen peroxide-treated lysates treated with phosphodiesterase 1 (0.5 μg/mL, 4 hr at 37ºC), or with tcPARG (5 μM, 4 hr at 37ºC ) using Poly/Mono-ADP Ribose (E6F6A) Rabbit mAb (upper), or GAPDH (D16H11) XP ® Rabbit mAb #5174 (lower). ANTI-MOUSE IGG (H+L), F(AB')2 FRAGMENT (ALEXA FLUOR® 555 Anti-Mouse IgG (H+L) F (ab') 2 Fragment was conjugated to Alexa Fluor 555 fluorescent dye under optimal conditions and formulated at 2 mg/ml. This F (ab') 2 fragment product results in less non-specific binding, as it lacks the Fc domain that can bind to the cells with Fcreceptors.
BIP ANTIBODY
Lyse cells by adding 1X SDS sample buffer (100 µl per well of 6-well plate or 500 µl for a 10 cm diameter plate). Immediately scrape the cells off the plate and transfer the extract to a microcentrifuge tube. Keep on ice. Sonicate for 10–15 sec to complete cell lysis and shear DNA (to reduce sample viscosity).CNPASE ANTIBODY
Immediately scrape the cells off the plate and transfer the extract to a microcentrifuge tube. Keep on ice. Sonicate for 10–15 sec to complete cell lysis and shear DNA (to reduce sample viscosity). Heat a 20 µl sample to 95–100°C for 5 min; cool on ice. Microcentrifugefor 5 min.
NRF2 ANTIBODY
Directions for Use: Wash membrane-bound HRP (antibody conjugate) three times for 5 minutes in TBST. Prepare 1X SignalFire™ ECL Reagent ( #6883) by diluting one part 2X Reagent A and one part 2X Reagent B (e.g. for 10 ml, add 5 ml Reagent A and 5 ml Reagent B). Mix well.MTOR ANTIBODY
The mTOR Antibody confirms silencing of mTOR expression, and the eIF4B Antibody is used to control for loading and siRNA specificity. Western blot analysis of extracts from 293 cells (starved for 16 hours), untreated or EGF-treated (100 ng/ml), using Phospho-mTOR (Ser2448) antibody #2971 (upper) or mTOR Antibody (lower). 1/3 Image Gallery. TBK1/NAK (D1B4) RABBIT MAB IP. Western blot analysis of HCT116 cell extracts, untreated (-) or TBK1/NAK knock-out (+), using TBK/NAK (D1B4) Rabbit mAb Antibody #3504 (upper) or β-actin (D6A8) Rabbit mAb #8457 (lower). Western blot analysis of extracts from various cell lines using TBK1/NAK (D1B4) Rabbit mAb. This product has been approved for use in this applicationby CST.
PHOSPHO-VASP (SER239) ANTIBODY Three phosphorylation sites, Ser157, Ser239, and Thr278, have been identified. Ser239 is the major PKG phosphorylation site while Ser157 is the major PKA phosphorylation site (4). Evidence suggests that VASP phosphorylation reduces its association with actin and has a negative effect on actin polymerization (5). CASPASE-8 (D35G2) RABBIT MAB Filter: WB. Western blot analysis of extracts from control HeLa cells (lane 1) or Caspase-8 knockout HeLa cells (lane 2) using Caspase-8 (D35G2) Rabbit mAb #4790 (upper), or β-actin (13E5) Rabbit mAb #4970 (lower). The absence of signal in the Caspase-8-knockout TAU (TAU46) MOUSE MAB Background Tau is a heterogeneous microtubule-associated protein that promotes and stabilizes microtubule assembly, especially in axons. Six isoforms with different amino-terminal inserts and different numbers of tandem repeats near the carboxy terminus have been identified, and tau is hyperphosphorylated at approximately 25 sites by Erk, GSK-3,and CDK5 (1,2).
GASDERMIN D ANTIBODY Lyse cells by adding 1X SDS sample buffer (100 µl per well of 6-well plate or 500 µl for a 10 cm diameter plate). Immediately scrape the cells off the plate and transfer the extract to a microcentrifuge tube. Keep on ice. Sonicate for 10–15 sec to complete cell lysis and shear DNA (to reduce sample viscosity). HUMAN IMMUNE CELL MARKER GUIDE WEB HANDOUT www.cellsignal.com Human Immune Cell Marker Guide T Cells CD3 + NK Cells CD56 and CD3– Cytotoxic Granzyme+ or erforin+ PB Immature/ Regulatory NK Cells CD56 high and CD16–and NCR+ CELL SIGNALING TECHNOLOGY (CST): ANTIBODIES, REAGENTSPRODUCTSSERVICESRESEARCHPROTEOMICSNEW AT CSTABOUT US An antibody shouldn’t be one of the variables in your experiment. Find out why customers rank CST highest for antibody specificity andsensitivity.
IN-CELL WESTERN™
In-Cell Western™ is a simple and cost effective means for quantification of intracellular signaling in whole cells. This assay involves seeding cells in microtiter plates followed by fixation/permeabilization and subsequent labeling with activation state-specific or control antibodies, infrared-conjugated secondary antibodies, and/or far-red DNA dye. TBK1/NAK (D1B4) RABBIT MAB IP. Western blot analysis of HCT116 cell extracts, untreated (-) or TBK1/NAK knock-out (+), using TBK/NAK (D1B4) Rabbit mAb Antibody #3504 (upper) or β-actin (D6A8) Rabbit mAb #8457 (lower). Western blot analysis of extracts from various cell lines using TBK1/NAK (D1B4) Rabbit mAb. This product has been approved for use in this applicationby CST.
PHOSPHO-SRC FAMILY (TYR416) (D49G4) RABBIT MAB Phospho-Src Family (Tyr416) (D49G4) Rabbit mAb detects endogenous levels of Src only when phosphorylated at Tyr416. The antibody may cross-react with other Src family members (Lyn, Fyn, Lck, Yes and Hck) when phosphorylated at equivalent sites. It may cross react with overexpressed phosphorylated RTKs. STAT1 (D1K9Y) RABBIT MAB IF. F. ChIP. Western blot analysis of extracts from A549 cells (lane 1) or STAT1 knock-out cells (lane 2) using Stat1 (D1K9Y) Rabbit mAb #14994 (upper), and β-actin (D6A8) Rabbit mAb #8457 (lower). The absence of signal in the STAT1 knock-out A549 cells confirms specificity of the antibody for STAT1. NANOG (D73G4) XP® RABBIT MAB Wash sections in wash buffer for 5 min. Block each section with 100–400 µl of preferred blocking solution for 1 hr at room temperature. Remove blocking solution and add 100–400 µl primary antibody diluted in SignalStain ® Antibody Diluent ( #8112) to each section. Incubate overnight at 4°C. FOXP3 (D6O8R) RABBIT MAB FoxP3 (D6O8R) Rabbit mAb recognizes endogenous levels of total FoxP3 protein. This antibody recognizes mouse FoxP3 protein and is also reactive with human FoxP3; however, this antibody is not suggested for immunohistochemical analysis of human tissues. Instead, FoxP3 (D2W8E™) Rabbit mAb (IHC Specific) #98377 is recommended for IHCanalysis of
PYRUVATE DEHYDROGENASE (C54G1) RABBIT MAB In mammalian cells, the pyruvate dehydrogenase complex is located in the mitochondrial matrix (1). This complex is comprised of three enzymes: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2) and dihydrolipoamide dehydrogenase (E3). Pyruvate dehydrogenase (E1) consists of two subunits: α and β. PHOSPHO-MYOSIN IIA (SER1943) ANTIBODY The antibody was pre-incubated with peptides corresponding to unphosphorylated Myosin IIa or Myosin IIa phosphorylated at Ser1943, as indicated. Western blot analysis of extracts from HeLa, A-431 and 293T cells, untreated or treated with λ phosphatase and calf intestinal phosphatase (CIP), using Phospho-Myosin IIa (Ser1943)Antibody (upper) or
ANTI-MOUSE IGG (H+L), F(AB')2 FRAGMENT (ALEXA FLUOR® 555 Anti-Mouse IgG (H+L) F (ab') 2 Fragment was conjugated to Alexa Fluor 555 fluorescent dye under optimal conditions and formulated at 2 mg/ml. This F (ab') 2 fragment product results in less non-specific binding, as it lacks the Fc domain that can bind to the cells with Fcreceptors.
CELL SIGNALING TECHNOLOGY (CST): ANTIBODIES, REAGENTSPRODUCTSSERVICESRESEARCHPROTEOMICSNEW AT CSTABOUT US An antibody shouldn’t be one of the variables in your experiment. Find out why customers rank CST highest for antibody specificity andsensitivity.
IN-CELL WESTERN™
In-Cell Western™ is a simple and cost effective means for quantification of intracellular signaling in whole cells. This assay involves seeding cells in microtiter plates followed by fixation/permeabilization and subsequent labeling with activation state-specific or control antibodies, infrared-conjugated secondary antibodies, and/or far-red DNA dye. TBK1/NAK (D1B4) RABBIT MAB IP. Western blot analysis of HCT116 cell extracts, untreated (-) or TBK1/NAK knock-out (+), using TBK/NAK (D1B4) Rabbit mAb Antibody #3504 (upper) or β-actin (D6A8) Rabbit mAb #8457 (lower). Western blot analysis of extracts from various cell lines using TBK1/NAK (D1B4) Rabbit mAb. This product has been approved for use in this applicationby CST.
PHOSPHO-SRC FAMILY (TYR416) (D49G4) RABBIT MAB Phospho-Src Family (Tyr416) (D49G4) Rabbit mAb detects endogenous levels of Src only when phosphorylated at Tyr416. The antibody may cross-react with other Src family members (Lyn, Fyn, Lck, Yes and Hck) when phosphorylated at equivalent sites. It may cross react with overexpressed phosphorylated RTKs. STAT1 (D1K9Y) RABBIT MAB IF. F. ChIP. Western blot analysis of extracts from A549 cells (lane 1) or STAT1 knock-out cells (lane 2) using Stat1 (D1K9Y) Rabbit mAb #14994 (upper), and β-actin (D6A8) Rabbit mAb #8457 (lower). The absence of signal in the STAT1 knock-out A549 cells confirms specificity of the antibody for STAT1. NANOG (D73G4) XP® RABBIT MAB Wash sections in wash buffer for 5 min. Block each section with 100–400 µl of preferred blocking solution for 1 hr at room temperature. Remove blocking solution and add 100–400 µl primary antibody diluted in SignalStain ® Antibody Diluent ( #8112) to each section. Incubate overnight at 4°C. FOXP3 (D6O8R) RABBIT MAB FoxP3 (D6O8R) Rabbit mAb recognizes endogenous levels of total FoxP3 protein. This antibody recognizes mouse FoxP3 protein and is also reactive with human FoxP3; however, this antibody is not suggested for immunohistochemical analysis of human tissues. Instead, FoxP3 (D2W8E™) Rabbit mAb (IHC Specific) #98377 is recommended for IHCanalysis of
PYRUVATE DEHYDROGENASE (C54G1) RABBIT MAB In mammalian cells, the pyruvate dehydrogenase complex is located in the mitochondrial matrix (1). This complex is comprised of three enzymes: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2) and dihydrolipoamide dehydrogenase (E3). Pyruvate dehydrogenase (E1) consists of two subunits: α and β. PHOSPHO-MYOSIN IIA (SER1943) ANTIBODY The antibody was pre-incubated with peptides corresponding to unphosphorylated Myosin IIa or Myosin IIa phosphorylated at Ser1943, as indicated. Western blot analysis of extracts from HeLa, A-431 and 293T cells, untreated or treated with λ phosphatase and calf intestinal phosphatase (CIP), using Phospho-Myosin IIa (Ser1943)Antibody (upper) or
ANTI-MOUSE IGG (H+L), F(AB')2 FRAGMENT (ALEXA FLUOR® 555 Anti-Mouse IgG (H+L) F (ab') 2 Fragment was conjugated to Alexa Fluor 555 fluorescent dye under optimal conditions and formulated at 2 mg/ml. This F (ab') 2 fragment product results in less non-specific binding, as it lacks the Fc domain that can bind to the cells with Fcreceptors.
BIP ANTIBODY
Lyse cells by adding 1X SDS sample buffer (100 µl per well of 6-well plate or 500 µl for a 10 cm diameter plate). Immediately scrape the cells off the plate and transfer the extract to a microcentrifuge tube. Keep on ice. Sonicate for 10–15 sec to complete cell lysis and shear DNA (to reduce sample viscosity). CST TECHNICAL DOCUMENTATION FOR SDS, COA, AND DATA SHEET Technical Support. Our scientists are at the bench daily to produce and validate our antibodies, so they have hands-on experience and knowledge of each antibody’s performance. Contact a Scientist. CYCLIN E1 (HE12) MOUSE MAB Lyse cells by adding 1X SDS sample buffer (100 µl per well of 6-well plate or 500 µl for a 10 cm diameter plate). Immediately scrape the cells off the plate and transfer the extract to a microcentrifuge tube. Keep on ice. Sonicate for 10–15 sec to complete cell lysis and shear DNA (to reduce sample viscosity).CNPASE ANTIBODY
Immediately scrape the cells off the plate and transfer the extract to a microcentrifuge tube. Keep on ice. Sonicate for 10–15 sec to complete cell lysis and shear DNA (to reduce sample viscosity). Heat a 20 µl sample to 95–100°C for 5 min; cool on ice. Microcentrifugefor 5 min.
NRF2 ANTIBODY
Directions for Use: Wash membrane-bound HRP (antibody conjugate) three times for 5 minutes in TBST. Prepare 1X SignalFire™ ECL Reagent ( #6883) by diluting one part 2X Reagent A and one part 2X Reagent B (e.g. for 10 ml, add 5 ml Reagent A and 5 ml Reagent B). Mix well. HES1 (D6P2U) RABBIT MAB Immunohistochemical analysis of paraffin-embedded CUTLL1 cell pellets, control (left) or Compound E-treated (right), using HES1 (D6P2U) Rabbit mAb. Western blot analysis of extracts from various cell lines using HES1 (D6P2U) Rabbit mAb. This product has been approved for use in this application by CST. ATF-6 (D4Z8V) RABBIT MAB Immunoprecipitation of ATF-6 from 293T cell extracts. Lane 1 is 10% input, lane 2 is Rabbit (DA1E) mAb IgG XP ® Isotype Control #3900, and lane 3 is ATF-6 (D4Z8V) Rabbit mAb. Western blot analysis was performed using ATF-6 (D4Z8V) Rabbit mAb. PHOSPHO-VASP (SER239) ANTIBODY Three phosphorylation sites, Ser157, Ser239, and Thr278, have been identified. Ser239 is the major PKG phosphorylation site while Ser157 is the major PKA phosphorylation site (4). Evidence suggests that VASP phosphorylation reduces its association with actin and has a negative effect on actin polymerization (5). POLY/MONO-ADP RIBOSE (E6F6A) RABBIT MAB Western blot analysis of Colo 205 cells treated (+) with combinations of the following treatments as indicated: hydrogen peroxide (500 μM, 5 min), hydrogen peroxide-treated lysates treated with phosphodiesterase 1 (0.5 μg/mL, 4 hr at 37ºC), or with tcPARG (5 μM, 4 hr at 37ºC ) using Poly/Mono-ADP Ribose (E6F6A) Rabbit mAb (upper), or GAPDH (D16H11) XP ® Rabbit mAb #5174 (lower). HUMAN IMMUNE CELL MARKER GUIDE WEB HANDOUT www.cellsignal.com Human Immune Cell Marker Guide T Cells CD3 + NK Cells CD56 and CD3– Cytotoxic Granzyme+ or erforin+ PB Immature/ Regulatory NK Cells CD56 high and CD16–and NCR+ CELL SIGNALING TECHNOLOGY (CST): ANTIBODIES, REAGENTSPRODUCTSSERVICESRESEARCHPROTEOMICSNEW AT CSTABOUT US An antibody shouldn’t be one of the variables in your experiment. Find out why customers rank CST highest for antibody specificity andsensitivity.
IN-CELL WESTERN™
In-Cell Western™ is a simple and cost effective means for quantification of intracellular signaling in whole cells. This assay involves seeding cells in microtiter plates followed by fixation/permeabilization and subsequent labeling with activation state-specific or control antibodies, infrared-conjugated secondary antibodies, and/or far-red DNA dye. TBK1/NAK (D1B4) RABBIT MAB IP. Western blot analysis of HCT116 cell extracts, untreated (-) or TBK1/NAK knock-out (+), using TBK/NAK (D1B4) Rabbit mAb Antibody #3504 (upper) or β-actin (D6A8) Rabbit mAb #8457 (lower). Western blot analysis of extracts from various cell lines using TBK1/NAK (D1B4) Rabbit mAb. This product has been approved for use in this applicationby CST.
PHOSPHO-SRC FAMILY (TYR416) (D49G4) RABBIT MAB Phospho-Src Family (Tyr416) (D49G4) Rabbit mAb detects endogenous levels of Src only when phosphorylated at Tyr416. The antibody may cross-react with other Src family members (Lyn, Fyn, Lck, Yes and Hck) when phosphorylated at equivalent sites. It may cross react with overexpressed phosphorylated RTKs. STAT1 (D1K9Y) RABBIT MAB IF. F. ChIP. Western blot analysis of extracts from A549 cells (lane 1) or STAT1 knock-out cells (lane 2) using Stat1 (D1K9Y) Rabbit mAb #14994 (upper), and β-actin (D6A8) Rabbit mAb #8457 (lower). The absence of signal in the STAT1 knock-out A549 cells confirms specificity of the antibody for STAT1. NANOG (D73G4) XP® RABBIT MAB Wash sections in wash buffer for 5 min. Block each section with 100–400 µl of preferred blocking solution for 1 hr at room temperature. Remove blocking solution and add 100–400 µl primary antibody diluted in SignalStain ® Antibody Diluent ( #8112) to each section. Incubate overnight at 4°C. FOXP3 (D6O8R) RABBIT MAB FoxP3 (D6O8R) Rabbit mAb recognizes endogenous levels of total FoxP3 protein. This antibody recognizes mouse FoxP3 protein and is also reactive with human FoxP3; however, this antibody is not suggested for immunohistochemical analysis of human tissues. Instead, FoxP3 (D2W8E™) Rabbit mAb (IHC Specific) #98377 is recommended for IHCanalysis of
PYRUVATE DEHYDROGENASE (C54G1) RABBIT MAB In mammalian cells, the pyruvate dehydrogenase complex is located in the mitochondrial matrix (1). This complex is comprised of three enzymes: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2) and dihydrolipoamide dehydrogenase (E3). Pyruvate dehydrogenase (E1) consists of two subunits: α and β. PHOSPHO-MYOSIN IIA (SER1943) ANTIBODY The antibody was pre-incubated with peptides corresponding to unphosphorylated Myosin IIa or Myosin IIa phosphorylated at Ser1943, as indicated. Western blot analysis of extracts from HeLa, A-431 and 293T cells, untreated or treated with λ phosphatase and calf intestinal phosphatase (CIP), using Phospho-Myosin IIa (Ser1943)Antibody (upper) or
ANTI-MOUSE IGG (H+L), F(AB')2 FRAGMENT (ALEXA FLUOR® 555 Anti-Mouse IgG (H+L) F (ab') 2 Fragment was conjugated to Alexa Fluor 555 fluorescent dye under optimal conditions and formulated at 2 mg/ml. This F (ab') 2 fragment product results in less non-specific binding, as it lacks the Fc domain that can bind to the cells with Fcreceptors.
CELL SIGNALING TECHNOLOGY (CST): ANTIBODIES, REAGENTSPRODUCTSSERVICESRESEARCHPROTEOMICSNEW AT CSTABOUT US An antibody shouldn’t be one of the variables in your experiment. Find out why customers rank CST highest for antibody specificity andsensitivity.
IN-CELL WESTERN™
In-Cell Western™ is a simple and cost effective means for quantification of intracellular signaling in whole cells. This assay involves seeding cells in microtiter plates followed by fixation/permeabilization and subsequent labeling with activation state-specific or control antibodies, infrared-conjugated secondary antibodies, and/or far-red DNA dye. TBK1/NAK (D1B4) RABBIT MAB IP. Western blot analysis of HCT116 cell extracts, untreated (-) or TBK1/NAK knock-out (+), using TBK/NAK (D1B4) Rabbit mAb Antibody #3504 (upper) or β-actin (D6A8) Rabbit mAb #8457 (lower). Western blot analysis of extracts from various cell lines using TBK1/NAK (D1B4) Rabbit mAb. This product has been approved for use in this applicationby CST.
PHOSPHO-SRC FAMILY (TYR416) (D49G4) RABBIT MAB Phospho-Src Family (Tyr416) (D49G4) Rabbit mAb detects endogenous levels of Src only when phosphorylated at Tyr416. The antibody may cross-react with other Src family members (Lyn, Fyn, Lck, Yes and Hck) when phosphorylated at equivalent sites. It may cross react with overexpressed phosphorylated RTKs. STAT1 (D1K9Y) RABBIT MAB IF. F. ChIP. Western blot analysis of extracts from A549 cells (lane 1) or STAT1 knock-out cells (lane 2) using Stat1 (D1K9Y) Rabbit mAb #14994 (upper), and β-actin (D6A8) Rabbit mAb #8457 (lower). The absence of signal in the STAT1 knock-out A549 cells confirms specificity of the antibody for STAT1. NANOG (D73G4) XP® RABBIT MAB Wash sections in wash buffer for 5 min. Block each section with 100–400 µl of preferred blocking solution for 1 hr at room temperature. Remove blocking solution and add 100–400 µl primary antibody diluted in SignalStain ® Antibody Diluent ( #8112) to each section. Incubate overnight at 4°C. FOXP3 (D6O8R) RABBIT MAB FoxP3 (D6O8R) Rabbit mAb recognizes endogenous levels of total FoxP3 protein. This antibody recognizes mouse FoxP3 protein and is also reactive with human FoxP3; however, this antibody is not suggested for immunohistochemical analysis of human tissues. Instead, FoxP3 (D2W8E™) Rabbit mAb (IHC Specific) #98377 is recommended for IHCanalysis of
PYRUVATE DEHYDROGENASE (C54G1) RABBIT MAB In mammalian cells, the pyruvate dehydrogenase complex is located in the mitochondrial matrix (1). This complex is comprised of three enzymes: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2) and dihydrolipoamide dehydrogenase (E3). Pyruvate dehydrogenase (E1) consists of two subunits: α and β. PHOSPHO-MYOSIN IIA (SER1943) ANTIBODY The antibody was pre-incubated with peptides corresponding to unphosphorylated Myosin IIa or Myosin IIa phosphorylated at Ser1943, as indicated. Western blot analysis of extracts from HeLa, A-431 and 293T cells, untreated or treated with λ phosphatase and calf intestinal phosphatase (CIP), using Phospho-Myosin IIa (Ser1943)Antibody (upper) or
ANTI-MOUSE IGG (H+L), F(AB')2 FRAGMENT (ALEXA FLUOR® 555 Anti-Mouse IgG (H+L) F (ab') 2 Fragment was conjugated to Alexa Fluor 555 fluorescent dye under optimal conditions and formulated at 2 mg/ml. This F (ab') 2 fragment product results in less non-specific binding, as it lacks the Fc domain that can bind to the cells with Fcreceptors.
BIP ANTIBODY
Lyse cells by adding 1X SDS sample buffer (100 µl per well of 6-well plate or 500 µl for a 10 cm diameter plate). Immediately scrape the cells off the plate and transfer the extract to a microcentrifuge tube. Keep on ice. Sonicate for 10–15 sec to complete cell lysis and shear DNA (to reduce sample viscosity). CST TECHNICAL DOCUMENTATION FOR SDS, COA, AND DATA SHEET Technical Support. Our scientists are at the bench daily to produce and validate our antibodies, so they have hands-on experience and knowledge of each antibody’s performance. Contact a Scientist. CYCLIN E1 (HE12) MOUSE MAB Lyse cells by adding 1X SDS sample buffer (100 µl per well of 6-well plate or 500 µl for a 10 cm diameter plate). Immediately scrape the cells off the plate and transfer the extract to a microcentrifuge tube. Keep on ice. Sonicate for 10–15 sec to complete cell lysis and shear DNA (to reduce sample viscosity).CNPASE ANTIBODY
Immediately scrape the cells off the plate and transfer the extract to a microcentrifuge tube. Keep on ice. Sonicate for 10–15 sec to complete cell lysis and shear DNA (to reduce sample viscosity). Heat a 20 µl sample to 95–100°C for 5 min; cool on ice. Microcentrifugefor 5 min.
NRF2 ANTIBODY
Directions for Use: Wash membrane-bound HRP (antibody conjugate) three times for 5 minutes in TBST. Prepare 1X SignalFire™ ECL Reagent ( #6883) by diluting one part 2X Reagent A and one part 2X Reagent B (e.g. for 10 ml, add 5 ml Reagent A and 5 ml Reagent B). Mix well. HES1 (D6P2U) RABBIT MAB Immunohistochemical analysis of paraffin-embedded CUTLL1 cell pellets, control (left) or Compound E-treated (right), using HES1 (D6P2U) Rabbit mAb. Western blot analysis of extracts from various cell lines using HES1 (D6P2U) Rabbit mAb. This product has been approved for use in this application by CST. ATF-6 (D4Z8V) RABBIT MAB Immunoprecipitation of ATF-6 from 293T cell extracts. Lane 1 is 10% input, lane 2 is Rabbit (DA1E) mAb IgG XP ® Isotype Control #3900, and lane 3 is ATF-6 (D4Z8V) Rabbit mAb. Western blot analysis was performed using ATF-6 (D4Z8V) Rabbit mAb. PHOSPHO-VASP (SER239) ANTIBODY Three phosphorylation sites, Ser157, Ser239, and Thr278, have been identified. Ser239 is the major PKG phosphorylation site while Ser157 is the major PKA phosphorylation site (4). Evidence suggests that VASP phosphorylation reduces its association with actin and has a negative effect on actin polymerization (5). POLY/MONO-ADP RIBOSE (E6F6A) RABBIT MAB Western blot analysis of Colo 205 cells treated (+) with combinations of the following treatments as indicated: hydrogen peroxide (500 μM, 5 min), hydrogen peroxide-treated lysates treated with phosphodiesterase 1 (0.5 μg/mL, 4 hr at 37ºC), or with tcPARG (5 μM, 4 hr at 37ºC ) using Poly/Mono-ADP Ribose (E6F6A) Rabbit mAb (upper), or GAPDH (D16H11) XP ® Rabbit mAb #5174 (lower). HUMAN IMMUNE CELL MARKER GUIDE WEB HANDOUT www.cellsignal.com Human Immune Cell Marker Guide T Cells CD3 + NK Cells CD56 and CD3– Cytotoxic Granzyme+ or erforin+ PB Immature/ Regulatory NK Cells CD56 high and CD16–and NCR+ CELL SIGNALING TECHNOLOGY (CST): ANTIBODIES, REAGENTSPRODUCTSSERVICESRESEARCHPROTEOMICSNEW AT CSTABOUT US An antibody shouldn’t be one of the variables in your experiment. Find out why customers rank CST highest for antibody specificity andsensitivity.
TBK1/NAK (D1B4) RABBIT MAB IP. Western blot analysis of HCT116 cell extracts, untreated (-) or TBK1/NAK knock-out (+), using TBK/NAK (D1B4) Rabbit mAb Antibody #3504 (upper) or β-actin (D6A8) Rabbit mAb #8457 (lower). Western blot analysis of extracts from various cell lines using TBK1/NAK (D1B4) Rabbit mAb. This product has been approved for use in this applicationby CST.
CASPASE-3 ANTIBODY
IP. IHC. Western blot analysis of extracts from HCT116 cells (lane 1) or CASP3 knock-out cells (lane 2) using Caspase-3 Antibody #9662 (upper), and α-Actinin (D6F6) XP® Rabbit mAb #6487 (lower). The absence of signal in the CASP3 knock-out HCT116 cells confirms specificity of the antibody for CASP3. Western blot analysis ofextracts from
RIPA BUFFER (10X)
2. Thaw 10x buffer at 24-30°C, mixing end-over-end. 3. Dilute 10X RIPA Buffer to a 1X solution using ddH2O. This product supplies enough 10X material to make 150mls of whole cell extract. 4. Chill 1X buffer on ice and add PMSF just prior to use. Note: CST recommends adding 1 STAT3 (124H6) MOUSE MAB ChIP. Chromatin immunoprecipitations were performed with cross-linked chromatin from Hep G2 cells starved overnight and treated with IL-6 (100 ng/ml) for 30 minutes, and either Stat3 (124H6) Mouse mAb or Normal Rabbit IgG #2729 using SimpleChIP ® Enzymatic Chromatin IP Kit (Magnetic Beads) #9003. The enriched DNA was quantified by real-time NANOG (D73G4) XP® RABBIT MAB Wash sections in wash buffer for 5 min. Block each section with 100–400 µl of preferred blocking solution for 1 hr at room temperature. Remove blocking solution and add 100–400 µl primary antibody diluted in SignalStain ® Antibody Diluent ( #8112) to each section. Incubate overnight at 4°C. EGF RECEPTOR (D38B1) XP® RABBIT MAB Western blot analysis of extracts from control Hela cells (lane 1), or EGFR knockout Hela cells (lane 2) using EGF Receptor (D38B1) XP® Rabbit mAb #4267, (upper) or #8457 β-Actin (D6A8) Rabbit mAb (lower). The absence of signal in EGFR-knockout Hela cells confirms specificity of the antibody for EGFR. PHOSPHO-4E-BP1 (THR37/46) (236B4) RABBIT MAB Phospho-4E-BP1 (Thr37/46) (236B4) Rabbit mAb detects endogenous levels of 4E-BP1 only when phosphorylated at Thr37 and/or Thr46. This antibody may cross-react with 4E-BP2 and 4E-BP3 when phosphorylated at equivalent sites. Non-specific staining has been observed in mitotic cells by immunofluorescence. POLY/MONO-ADP RIBOSE (E6F6A) RABBIT MAB Western blot analysis of Colo 205 cells treated (+) with combinations of the following treatments as indicated: hydrogen peroxide (500 μM, 5 min), hydrogen peroxide-treated lysates treated with phosphodiesterase 1 (0.5 μg/mL, 4 hr at 37ºC), or with tcPARG (5 μM, 4 hr at 37ºC ) using Poly/Mono-ADP Ribose (E6F6A) Rabbit mAb (upper), or GAPDH (D16H11) XP ® Rabbit mAb #5174 (lower). PYRUVATE DEHYDROGENASE (C54G1) RABBIT MAB In mammalian cells, the pyruvate dehydrogenase complex is located in the mitochondrial matrix (1). This complex is comprised of three enzymes: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2) and dihydrolipoamide dehydrogenase (E3). Pyruvate dehydrogenase (E1) consists of two subunits: α and β. CELL SIGNALING TECHNOLOGY (CST): ANTIBODIES, REAGENTSPRODUCTSSERVICESRESEARCHPROTEOMICSNEW AT CSTABOUT US An antibody shouldn’t be one of the variables in your experiment. Find out why customers rank CST highest for antibody specificity andsensitivity.
TBK1/NAK (D1B4) RABBIT MAB IP. Western blot analysis of HCT116 cell extracts, untreated (-) or TBK1/NAK knock-out (+), using TBK/NAK (D1B4) Rabbit mAb Antibody #3504 (upper) or β-actin (D6A8) Rabbit mAb #8457 (lower). Western blot analysis of extracts from various cell lines using TBK1/NAK (D1B4) Rabbit mAb. This product has been approved for use in this applicationby CST.
CASPASE-3 ANTIBODY
IP. IHC. Western blot analysis of extracts from HCT116 cells (lane 1) or CASP3 knock-out cells (lane 2) using Caspase-3 Antibody #9662 (upper), and α-Actinin (D6F6) XP® Rabbit mAb #6487 (lower). The absence of signal in the CASP3 knock-out HCT116 cells confirms specificity of the antibody for CASP3. Western blot analysis ofextracts from
RIPA BUFFER (10X)
2. Thaw 10x buffer at 24-30°C, mixing end-over-end. 3. Dilute 10X RIPA Buffer to a 1X solution using ddH2O. This product supplies enough 10X material to make 150mls of whole cell extract. 4. Chill 1X buffer on ice and add PMSF just prior to use. Note: CST recommends adding 1 STAT3 (124H6) MOUSE MAB ChIP. Chromatin immunoprecipitations were performed with cross-linked chromatin from Hep G2 cells starved overnight and treated with IL-6 (100 ng/ml) for 30 minutes, and either Stat3 (124H6) Mouse mAb or Normal Rabbit IgG #2729 using SimpleChIP ® Enzymatic Chromatin IP Kit (Magnetic Beads) #9003. The enriched DNA was quantified by real-time NANOG (D73G4) XP® RABBIT MAB Wash sections in wash buffer for 5 min. Block each section with 100–400 µl of preferred blocking solution for 1 hr at room temperature. Remove blocking solution and add 100–400 µl primary antibody diluted in SignalStain ® Antibody Diluent ( #8112) to each section. Incubate overnight at 4°C. EGF RECEPTOR (D38B1) XP® RABBIT MAB Western blot analysis of extracts from control Hela cells (lane 1), or EGFR knockout Hela cells (lane 2) using EGF Receptor (D38B1) XP® Rabbit mAb #4267, (upper) or #8457 β-Actin (D6A8) Rabbit mAb (lower). The absence of signal in EGFR-knockout Hela cells confirms specificity of the antibody for EGFR. PHOSPHO-4E-BP1 (THR37/46) (236B4) RABBIT MAB Phospho-4E-BP1 (Thr37/46) (236B4) Rabbit mAb detects endogenous levels of 4E-BP1 only when phosphorylated at Thr37 and/or Thr46. This antibody may cross-react with 4E-BP2 and 4E-BP3 when phosphorylated at equivalent sites. Non-specific staining has been observed in mitotic cells by immunofluorescence. POLY/MONO-ADP RIBOSE (E6F6A) RABBIT MAB Western blot analysis of Colo 205 cells treated (+) with combinations of the following treatments as indicated: hydrogen peroxide (500 μM, 5 min), hydrogen peroxide-treated lysates treated with phosphodiesterase 1 (0.5 μg/mL, 4 hr at 37ºC), or with tcPARG (5 μM, 4 hr at 37ºC ) using Poly/Mono-ADP Ribose (E6F6A) Rabbit mAb (upper), or GAPDH (D16H11) XP ® Rabbit mAb #5174 (lower). PYRUVATE DEHYDROGENASE (C54G1) RABBIT MAB In mammalian cells, the pyruvate dehydrogenase complex is located in the mitochondrial matrix (1). This complex is comprised of three enzymes: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2) and dihydrolipoamide dehydrogenase (E3). Pyruvate dehydrogenase (E1) consists of two subunits: α and β.RIPA BUFFER (10X)
2. Thaw 10x buffer at 24-30°C, mixing end-over-end. 3. Dilute 10X RIPA Buffer to a 1X solution using ddH2O. This product supplies enough 10X material to make 150mls of whole cell extract. 4. Chill 1X buffer on ice and add PMSF just prior to use. Note: CST recommends adding 1 CELL LYSIS BUFFER (10X) Solutions and Reagents. 20 mM Tris-HCl (pH 7.5), 150 mM NaCl, 1 mM Na 2 EDTA, 1 mM EGTA, 1% Triton, 2.5 mM sodium pyrophosphate, 1 mM beta-glycerophosphate, 1 mM Na 3 VO 4, 1 µg/ml leupeptinNote: CST recommends adding 1 mM PMSF immediately before use.. Storage. This product is stable for 24 months when stored at -20°C. Cell Lysis Buffer can be stored at 4°C for a short period of C-MYC (D84C12) RABBIT MAB Confocal immunofluorescent analysis of HeLa cells, mock-transfected (left) or transfected with SignalSilence ® c-Myc siRNA I #6341 (right), using c-Myc (D84C12) Rabbit mAb (green). Actin filaments have been labeled wth DY-554 phalloidin (red). Western blot analysis of extracts from control HEK293 cells (lane 1) or c-Myc knockout HEK293cells
PHOSPHO-SRC FAMILY (TYR416) ANTIBODY Phospho-Src Family (Tyr416) Antibody detects endogenous levels of Src only when phosphorylated at tyrosine 416. The antibody may cross-react with other Src family members (Lyn, Fyn, Lck, Yes and Hck) when phosphorylated at equivalent sites. It does not cross-react with Src phosphorylated at tyrosine 527.LC3B ANTIBODY
Background Autophagy is a catabolic process for the autophagosomic-lysosomal degradation of bulk cytoplasmic contents (1,2). Autophagy is generally activated by conditions of nutrient deprivation, but it has also been associated with a number of physiological processes including development, differentiation, neurodegenerative diseases, infection, and cancer (3). NANOG (D73G4) XP® RABBIT MAB Wash sections in wash buffer for 5 min. Block each section with 100–400 µl of preferred blocking solution for 1 hr at room temperature. Remove blocking solution and add 100–400 µl primary antibody diluted in SignalStain ® Antibody Diluent ( #8112) to each section. Incubate overnight at 4°C. ACETYL-P53 (LYS379) ANTIBODY Lyse cells by adding 1X SDS sample buffer (100 µl per well of 6-well plate or 500 µl for a 10 cm diameter plate). Immediately scrape the cells off the plate and transfer the extract to a microcentrifuge tube. Keep on ice. Sonicate for 10–15 sec to complete cell lysis and shear DNA (to reduce sample viscosity). PHOSPHO-4E-BP1 (THR37/46) (236B4) RABBIT MAB Phospho-4E-BP1 (Thr37/46) (236B4) Rabbit mAb detects endogenous levels of 4E-BP1 only when phosphorylated at Thr37 and/or Thr46. This antibody may cross-react with 4E-BP2 and 4E-BP3 when phosphorylated at equivalent sites. Non-specific staining has been observed in mitotic cells by immunofluorescence. ANTI-RABBIT IGG, HRP-LINKED ANTIBODY Designed for use with rabbit polyclonal and monoclonal antibodies, this affinity purified goat anti-rabbit IgG (heavy and light chain) antibody is conjugated to horseradish peroxidase (HRP) for chemiluminescent detection. This product is thoroughly validated with CST primary antibodies and will work optimally with the CST westernimmunoblotting
ANTI-MOUSE IGG (H+L), F(AB')2 FRAGMENT (ALEXA FLUOR® 555 Anti-Mouse IgG (H+L) F (ab') 2 Fragment was conjugated to Alexa Fluor 555 fluorescent dye under optimal conditions and formulated at 2 mg/ml. This F (ab') 2 fragment product results in less non-specific binding, as it lacks the Fc domain that can bind to the cells with Fcreceptors.
×
GO TO YOUR REGIONAL SITE? Would you like to visit your country specific website?YES NO
Save This Selection
×
VIEW IN ENGLISH?
View in English?
YES NO
Save This Selection
Country/Region (USA) Language: Open a Technical Support CaseContact
Us ®">PhosphoSitePlus®register log in
__ shopping cart (0)__ __ 0 __
Products
#3715#9941#9942#9391#3004#14989#3014#4590#4593#8508#9071#4331#13390#4332#3078#2225#9508#8592#14071#9496#5243#9606#12602#9429#9381#8781#8859#6949#12742#9930#12105#6947#12703#12242#14155#13627#3814#2573#8916#8900#5236#5218#12157#6486#8335#2459#5055#2321#3792#8667#9908#8909#8628#2022#2021#9934__
Products Content __
Country/Region (USA) Language EN* Home
* About Us
Back to Main Menu
* About Us
* Technical Support
* Careers
* Location & Shipping Information* Leadership Team
* Corporate Social Responsibility * Conferences & Events* CST Media Room
* Antibody Reproducibility* Applications
* Publications by CST Scientists * Product Literature* Certifications
* Contact Information* Products
Back to Main Menu
BY PRODUCT TYPE
* Primary Antibodies* Antibody Samplers
* Secondary Antibodies * Antibody Conjugates* ELISA Kits
* ChIP Kits & Reagents * Proteomic Analysis Products * Cellular Assay Kits* WB & IP Reagents
* siRNA
* Activators & Inhibitors * Experimental Controls* Buffers & Dyes
BY APPLICATION
* Western Blotting (WB) * Immunoprecipitation (IP) * Immunohistochemistry (IHC) * Immunofluorescence (IF) * Flow Cytometry (F) * Chromatin Immunoprecipitation (ChIP) * Sandwich Immunoassays (ELISA)* Services
Back to Main Menu
* Customized Solutions * PTMScan® Proteomics Services * Custom Antibody Conjugation Services* Research
Back to Main Menu
* Research
* CST Pathways
* Cancer Research
* Webinars & Videos
* Protein Kinases: Introduction * Cellular Landscapes * Poster Presentations * Useful Web Resources * Reference Table Resources * Protein and Pathway Abbreviations* Protocols
* Frequently Asked Questions (FAQs) * Control Treatments by Target * Tutorials & Application Guides* Proteomics
Back to Main Menu
* Proteomics Services* Proteomics Kits
* Responsibility
Back to Main Menu
* Commitment to Science * Commitment to Employees * Community Investment* Sustainability
* Commitment to the Arts* New At CST
Back to Main Menu
* Products
* Careers
* Current Promotions * Blog - Lab Expectations Introductory Promo Offer for New CUT&RUN Products!* | Learn More >>G1/S AND G2M
CELL CYCLE CONTROL
Signaling Pathways
Download
SEARCH INTERACTIVE PATHWAYSExplore
BEHIND THE ABS
Meet Dr. Cell Death!Watch Now
New Products
Promotions
Events & Webinars
Responsibility
PhosphoSitePlus
Tech Support
IMMUNOLOGY
AND IMMUNO-ONCOLOGY
Antibodies, reagents, and resources, such as pathways, protocols & videos, to help you accelerate your research. NEUROSCIENCE AND NEURODEGENERATION Reagents and resources to decipher neurodegeneration and deepen your understanding of the brain. STARTER GUIDE FOR CANCER EPIGENETICS Important epi biomarkers, regulators, and histone modifications for several types of cancer. RNA REGULATION & EPITRANSCRIPTOMICS IN DISEASE Learn more about the link between RNA processing and modifications with disease progression. DECIPHERING FIBROSIS: ON DEMAND Exploring the biological drivers of fibrotic disease in the liver andheart. Watch now.
TIRED OF MOUSE-ON-MOUSE BACKGROUND STAINING? Get the data you need without the background you don't by using IHC-validated rabbit mAbs.VISIT US AT
* __
* __
* __
* __
* __
ABOUT
* About Us
* Products
* Services
* Research
* Proteomics
* New At CST
* BLOG – LAB EXPECTATIONSLEGAL
* Trademark Info
* Privacy Policy
* Privacy Shield
* Cookie Policy
* Terms & ConditionsSUPPORT
* Order Information
Open a Technical Support CaseLOCATIONS
Cell Signaling Technology3 Trask Lane
Danvers, MA 01923
Global Offices
JOBS
* Careers
Discover © 2020 Cell Signaling Technology, Inc. All Rights Reserved. Email:info@cellsignal.com
×
SELECT YOUR COUNTRY/REGION Changing to another country might result in loss of shopping cart.Country/Region
Continue
Feedback
×
Details
Copyright © 2024 ArchiveBay.com. All rights reserved. Terms of Use | Privacy Policy | DMCA | 2021 | Feedback | Advertising | RSS 2.0