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HRP Conjugated GAPDH Recombinant Rabbit Monoclonal Antibody [SA30-01]

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Catalog# HA721131

HRP Conjugated GAPDH Recombinant Rabbit Monoclonal Antibody [SA30-01]

Application

  • WB

  • IHC

Reactivity

  • Human

  • Mouse

  • Rat

This product has been cited in peer reviewed publications, see list HERE

概述

产品名称

HRP Conjugated GAPDH Recombinant Rabbit Monoclonal Antibody [SA30-01]

抗体类型

Recombinant Rabbit monoclonal Antibody

免疫原

Recombinant protein within mouse GAPDH aa 94-333 / 333.

种属反应性

Human, Mouse, Rat

验证应用

WB, IHC

分子量

Predicted band size: 36 kDa

阳性对照

HepG2 cell lysates, PC-12 cell lysates, NIH/3T3 cell lysates, THP-1 cell lysate, MCF-7 cell lysate, RH-35 cell lysate, HepG2 cell lysate, PC-12 cell lysate, L6 cell lysate, RAW264.7 cell lysate, A549 cell lysate, PMVEC cell lysate, NIH/3T3 cell lysate, B16F1 cell lysate.

偶联

HRP

克隆号

SA30-01

RRID

AB_3072255

产品特性

形态

Liquid

浓度

0.5ug/ul

存放说明

Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.

存储缓冲液

PBS (pH7.4), 0.1% BSA, 40% Glycerol.

亚型

IgG

纯化方式

Protein A affinity purified.

应用稀释度

  • WB

  • 1:2,500-1:20,000

  • IHC

  • 1:50-1:200

发表文章中的应用

WB 查看 2 篇文献如下

发表文章中的种属

Mouse 查看 1 篇文献如下
Rat 查看 1 篇文献如下

靶点

功能

Has both glyceraldehyde-3-phosphate dehydrogenase and nitrosylase activities, thereby playing a role in glycolysis and nuclear functions, respectively. Participates in nuclear events including transcription, RNA transport, DNA replication and apoptosis. Nuclear functions are probably due to the nitrosylase activity that mediates cysteine S-nitrosylation of nuclear target proteins such as SIRT1, HDAC2 and PRKDC. Modulates the organization and assembly of the cytoskeleton. Facilitates the CHP1-dependent microtubule and membrane associations through its ability to stimulate the binding of CHP1 to microtubules. Glyceraldehyde-3-phosphate dehydrogenase is a key enzyme in glycolysis that catalyzes the first step of the pathway by converting D-glyceraldehyde 3-phosphate (G3P) into 3-phospho-D-glyceroyl phosphate. Component of the GAIT (gamma interferon-activated inhibitor of translation) complex which mediates interferon-gamma-induced transcript-selective translation inhibition in inflammation processes. Upon interferon-gamma treatment assembles into the GAIT complex which binds to stem loop-containing GAIT elements in the 3'-UTR of diverse inflammatory mRNAs (such as ceruplasmin) and suppresses their translation.

背景文献

1. "High-resolution structure of human D-glyceraldehyde-3-phosphate dehydrogenase."Jenkins J.L., Tanner J.J.Acta Crystallogr. D 62:290-301(2006)

2. "Structural analysis of human liver glyceraldehyde-3-phosphate dehydrogenase."Ismail S.A., Park H.W.Acta Crystallogr. D 61:1508-1513(2005)

亚细胞定位

Cytoplasm, Nucleus, Membrane.

UNIPROT

SwissProt: P04406 Human

SwissProt: P16858 Mouse

SwissProt: P04797 Rat

别名

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展开

图片

  • Western blot analysis of GAPDH on HepG2 cell lysates with Rabbit anti-GAPDH antibody (<a href="/products/HA721131" style="font-weight: bold;text-decoration: underline;">HA721131</a>) at different dilutions.<br /><br />Lysates/proteins at 10 µg/Lane.<br /><br />Predicted band size: 36 kDa<br />Observed band size: 36 kDa<br /><br />Exposure time: 30 seconds;<br /><br />10% SDS-PAGE gel.<br /><br />Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (<a href="/products/HA721131" style="font-weight: bold;text-decoration: underline;">HA721131</a>) at different dilutions were used in 5% NFDM/TBST at room temperature for 2 hours.

    Western blot analysis of GAPDH on HepG2 cell lysates with Rabbit anti-GAPDH antibody (HA721131) at different dilutions.

    Lysates/proteins at 10 µg/Lane.

    Predicted band size: 36 kDa
    Observed band size: 36 kDa

    Exposure time: 30 seconds;

    10% SDS-PAGE gel.

    Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA721131) at different dilutions were used in 5% NFDM/TBST at room temperature for 2 hours.

  • Western blot analysis of GAPDH on PC-12 cell lysates with Rabbit anti-GAPDH antibody (<a href="/products/HA721131" style="font-weight: bold;text-decoration: underline;">HA721131</a>) at different dilutions.<br /><br />Lysates/proteins at 10 µg/Lane.<br /><br />Predicted band size: 36 kDa<br />Observed band size: 36 kDa<br /><br />Exposure time: 30 seconds;<br /><br />10% SDS-PAGE gel.<br /><br />Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (<a href="/products/HA721131" style="font-weight: bold;text-decoration: underline;">HA721131</a>) at different dilutions were used in 5% NFDM/TBST at room temperature for 2 hours.

    Western blot analysis of GAPDH on PC-12 cell lysates with Rabbit anti-GAPDH antibody (HA721131) at different dilutions.

    Lysates/proteins at 10 µg/Lane.

    Predicted band size: 36 kDa
    Observed band size: 36 kDa

    Exposure time: 30 seconds;

    10% SDS-PAGE gel.

    Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA721131) at different dilutions were used in 5% NFDM/TBST at room temperature for 2 hours.

  • Immunohistochemical analysis of paraffin-embedded human liver tissue with Rabbit anti-GAPDH antibody (<a href="/products/HA721131" style="font-weight: bold;text-decoration: underline;">HA721131</a>) at 1/50 dilution.<br /><br />The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH<sub>2</sub>O and PBS, and then probed with the primary antibody (<a href="/products/HA721131" style="font-weight: bold;text-decoration: underline;">HA721131</a>) at 1/50 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

    Immunohistochemical analysis of paraffin-embedded human liver tissue with Rabbit anti-GAPDH antibody (HA721131) at 1/50 dilution.

    The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721131) at 1/50 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

  • Western blot analysis of GAPDH on NIH/3T3 cell lysates with Rabbit anti-GAPDH antibody (<a href="/products/HA721131" style="font-weight: bold;text-decoration: underline;">HA721131</a>) at different dilutions.<br /><br />Lysates/proteins at 10 µg/Lane.<br /><br />Predicted band size: 36 kDa<br />Observed band size: 36 kDa<br /><br />Exposure time: 30 seconds;<br /><br />10% SDS-PAGE gel.<br /><br />Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (<a href="/products/HA721131" style="font-weight: bold;text-decoration: underline;">HA721131</a>) at different dilutions were used in 5% NFDM/TBST at room temperature for 2 hours.

    Western blot analysis of GAPDH on NIH/3T3 cell lysates with Rabbit anti-GAPDH antibody (HA721131) at different dilutions.

    Lysates/proteins at 10 µg/Lane.

    Predicted band size: 36 kDa
    Observed band size: 36 kDa

    Exposure time: 30 seconds;

    10% SDS-PAGE gel.

    Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA721131) at different dilutions were used in 5% NFDM/TBST at room temperature for 2 hours.

  • Western blot analysis of GAPDH on different lysates with Rabbit anti-GAPDH antibody (<a href="/products/HA721131" style="font-weight: bold;text-decoration: underline;">HA721131</a>) at 1/10,000 dilution.<br /><br />Lane 1: THP-1 cell lysate<br />Lane 2: MCF-7 cell lysate<br />Lane 3: RH-35 cell lysate<br />Lane 4: HepG2 cell lysate<br />Lane 5: PC-12 cell lysate<br />Lane 6: L6 cell lysate<br />Lane 7: RAW264.7 cell lysate<br />Lane 8: A549 cell lysate<br />Lane 9: PMVEC cell lysate<br />Lane 10: NIH/3T3 cell lysate<br />Lane 11: B16F1 cell lysate<br /><br />Lysates/proteins at 10 µg/Lane.<br /><br />Predicted band size: 36 kDa<br />Observed band size: 36 kDa<br /><br />Exposure time: 30 seconds;<br /><br />10% SDS-PAGE gel.<br /><br />Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (<a href="/products/HA721131" style="font-weight: bold;text-decoration: underline;">HA721131</a>) at 1/10,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours.

    Western blot analysis of GAPDH on different lysates with Rabbit anti-GAPDH antibody (HA721131) at 1/10,000 dilution.

    Lane 1: THP-1 cell lysate
    Lane 2: MCF-7 cell lysate
    Lane 3: RH-35 cell lysate
    Lane 4: HepG2 cell lysate
    Lane 5: PC-12 cell lysate
    Lane 6: L6 cell lysate
    Lane 7: RAW264.7 cell lysate
    Lane 8: A549 cell lysate
    Lane 9: PMVEC cell lysate
    Lane 10: NIH/3T3 cell lysate
    Lane 11: B16F1 cell lysate

    Lysates/proteins at 10 µg/Lane.

    Predicted band size: 36 kDa
    Observed band size: 36 kDa

    Exposure time: 30 seconds;

    10% SDS-PAGE gel.

    Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA721131) at 1/10,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours.

  • Immunohistochemical analysis of paraffin-embedded mouse liver tissue with Rabbit anti-GAPDH antibody (<a href="/products/HA721131" style="font-weight: bold;text-decoration: underline;">HA721131</a>) at 1/200 dilution.<br /><br />The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH<sub>2</sub>O and PBS, and then probed with the primary antibody (<a href="/products/HA721131" style="font-weight: bold;text-decoration: underline;">HA721131</a>) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

    Immunohistochemical analysis of paraffin-embedded mouse liver tissue with Rabbit anti-GAPDH antibody (HA721131) at 1/200 dilution.

    The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721131) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

  • Immunohistochemical analysis of paraffin-embedded rat liver tissue with Rabbit anti-GAPDH antibody (<a href="/products/HA721131" style="font-weight: bold;text-decoration: underline;">HA721131</a>) at 1/200 dilution.<br /><br />The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH<sub>2</sub>O and PBS, and then probed with the primary antibody (<a href="/products/HA721131" style="font-weight: bold;text-decoration: underline;">HA721131</a>) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

    Immunohistochemical analysis of paraffin-embedded rat liver tissue with Rabbit anti-GAPDH antibody (HA721131) at 1/200 dilution.

    The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721131) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

请注意: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"

引文

Filter:
  1. WB

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