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HIF-1 alpha Recombinant Rabbit Monoclonal Antibody [JE75-33]

RMB: 900 特惠 1500

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Catalog# HA721997

HIF-1 alpha Recombinant Rabbit Monoclonal Antibody [JE75-33]

Application

  • WB

  • IF-Cell

Reactivity

  • Human

Conjugation

  • unconjugated

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

概述

产品名称

HIF-1 alpha Recombinant Rabbit Monoclonal Antibody [JE75-33]

抗体类型

Recombinant Rabbit monoclonal Antibody

免疫原

Recombinant protein within Human HIF-1 alpha aa 251-550 / 826.

种属反应性

Human

验证应用

WB, IF-Cell

分子量

Predicted band size: 93 kDa

阳性对照

HeLa treated with 0.5mM CoCl2 for 6 hours cell lysate, HeLa cells treated with or without 500μM CoCl2 for 24 hours.

偶联

unconjugated

克隆号

JE75-33

RRID

AB_3096587

反应性数据

WB IF-Cell
Human
Tested Tested
Tested Tested
Mouse
Tested
Not Recommended
Rat
Tested
Fish
Tested

产品特性

形态

Liquid

浓度

存放说明

Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term.

存储缓冲液

1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.

亚型

IgG

纯化方式

Protein A affinity purified.

应用稀释度

  • WB

  • 1:5,000

  • IF-Cell

  • 1:100

靶点

功能

Hypoxia-inducible factor 1-alpha, also known as HIF-1-alpha, is a subunit of a heterodimeric transcription factor hypoxia-inducible factor 1 (HIF-1) that is encoded by the HIF1A gene. The Nobel Prize in Physiology or Medicine 2019 was awarded for the discovery of HIF. HIF1A is a basic helix-loop-helix PAS domain containing protein, and is considered as the master transcriptional regulator of cellular and developmental response to hypoxia. The dysregulation and overexpression of HIF1A by either hypoxia or genetic alternations have been heavily implicated in cancer biology, as well as a number of other pathophysiologies, specifically in areas of vascularization and angiogenesis, energy metabolism, cell survival, and tumor invasion. Two other alternative transcripts encoding different isoforms have been identified.

背景文献

1. Korbecki J et al. Chronic and Cycling Hypoxia: Drivers of Cancer Chronic Inflammation through HIF-1 and NF-κB Activation: A Review of the Molecular Mechanisms. Int J Mol Sci. 2021 Oct

2. Infantino V et al. Cancer Cell Metabolism in Hypoxia: Role of HIF-1 as Key Regulator and Therapeutic Target. Int J Mol Sci. 2021 May

亚细胞定位

Cytoplasm, Nucleus, Nucleus speckle.

UNIPROT

SwissProt: Q16665 Human

SwissProt: Q61221 Mouse

SwissProt: O35800 Rat

别名

ARNT interacting protein antibody

ARNT-interacting protein antibody

Basic helix loop helix PAS protein MOP1 antibody

Basic-helix-loop-helix-PAS protein MOP1 antibody

bHLHe78 antibody

Class E basic helix-loop-helix protein 78 antibody

HIF 1A antibody

HIF 1alpha antibody

HIF-1-alpha antibody

HIF-1alpha antibody

展开

图片

  • <span style="font-weight: bold;">☑ Cell treatment (CT)</span><br /><br />Western blot analysis of HIF-1 alpha on different lysates with Rabbit anti-HIF-1 alpha antibody (<a href="/products/HA721997" style="font-weight: bold;text-decoration: underline;">HA721997</a>) at 1/5,000 dilution.<br /><br />Lane 1: HeLa cell lysate (15 µg/Lane)<br />Lane 2: HeLa treated with 0.5mM CoCl2 for 6 hours cell lysate (With sonication) (15 µg/Lane)<br />Lane 3: HeLa treated with 0.5mM CoCl2 for 6 hours cell lysate (Without sonication) (15 µg/Lane)<br /><br />Predicted band size: 93 kDa<br />Observed band size: 120 kDa<br /><br />Exposure time: 10 seconds; ECL: K1801;<br />4-20% 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/HA721997" style="font-weight: bold;text-decoration: underline;">HA721997</a>) at 1/5,000 dilution was used in K1803 at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (<a href="/products/HA1001" style="font-weight: bold;text-decoration: underline;">HA1001</a>) at 1/50,000 dilution was used for 1 hour at room temperature.

    ☑ Cell treatment (CT)

    Western blot analysis of HIF-1 alpha on different lysates with Rabbit anti-HIF-1 alpha antibody (HA721997) at 1/5,000 dilution.

    Lane 1: HeLa cell lysate (15 µg/Lane)
    Lane 2: HeLa treated with 0.5mM CoCl2 for 6 hours cell lysate (With sonication) (15 µg/Lane)
    Lane 3: HeLa treated with 0.5mM CoCl2 for 6 hours cell lysate (Without sonication) (15 µg/Lane)

    Predicted band size: 93 kDa
    Observed band size: 120 kDa

    Exposure time: 10 seconds; ECL: K1801;
    4-20% 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 (HA721997) at 1/5,000 dilution was used in K1803 at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.

  • <span style="font-weight: bold;">☑ Cell treatment (CT)</span><br /><br />Immunocytochemistry analysis of HeLa cells treated with or without 500μM CoCl2 for 24 hours labeling HIF-1 alpha with Rabbit anti-HIF-1 alpha antibody (<a href="/products/HA721997" style="font-weight: bold;text-decoration: underline;">HA721997</a>) at 1/100 dilution.<br /><br />Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-HIF-1 alpha antibody (<a href="/products/HA721997" style="font-weight: bold;text-decoration: underline;">HA721997</a>) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor&trade; 488, <a href="/products/HA1121" style="font-weight: bold;text-decoration: underline;">HA1121</a>) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.

    ☑ Cell treatment (CT)

    Immunocytochemistry analysis of HeLa cells treated with or without 500μM CoCl2 for 24 hours labeling HIF-1 alpha with Rabbit anti-HIF-1 alpha antibody (HA721997) at 1/100 dilution.

    Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-HIF-1 alpha antibody (HA721997) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.

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

引文

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