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Merck
CN

SAB3500566

Sigma-Aldrich

Anti-TCF12 antibody produced in rabbit

affinity isolated antibody, buffered aqueous solution

别名:

Anti-HEB, Anti-HTF4, Anti-bHLHb20

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关于此项目

UNSPSC代码:
12352203
NACRES:
NA.41
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生物来源

rabbit

质量水平

偶联物

unconjugated

抗体形式

affinity isolated antibody

抗体产品类型

primary antibodies

克隆

polyclonal

表单

buffered aqueous solution

种属反应性

human, mouse, rat

技术

immunocytochemistry: suitable
indirect ELISA: suitable
western blot: suitable

NCBI登记号

UniProt登记号

运输

dry ice

储存温度

−20°C

靶向翻译后修饰

unmodified

基因信息

human ... TCF12(6938)

一般描述

Transcription factor 12 (TCF12) is a class I member of helix-loop-helix (HLH) protein family, encodes for class II basic helix-loop-helix protein (bHLHb) transcription factor. In human chromosome, the gene TCF12 is localized on 15q21.3.

免疫原

TCF12 antibody was raised against a 19 amino acid peptide near the amino terminus of human TCF12.

应用

Anti-TCF12 antibody produced in rabbit has been used in immunoblotting.

生化/生理作用

Transcription factor 12 (TCF12) represses E-cadherin expression and thereby controls metastasis of colorectal cancer cells. TCF12 might play a role in controlling the proliferation of neural stem cells and progenitor cells. TCF12-TWIST1 (twist family bHLH transcription factor 1) heterodimers is required for the development of normal coronal suture. Mutations in the TCF12 heterodimer causes coronal craniosynostosis. TCF12 is critically required for regulating human mesodermal and hematopoietic specification in the early development. Mutations in TCF12 affects the transcriptional activity and leads to anaplastic oligodendroglioma, a rare brain tumor.

特点和优势

Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.

外形

Supplied in PBS with 0.02% sodium azide.

其他说明

The action of this antibody can be blocked using blocking peptide SBP3500566.

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储存分类代码

10 - Combustible liquids

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis
Sharma VP, et al.
Nature Genetics, 45(3), 304-304 (2013)
TCF-1 and HEB cooperate to establish the epigenetic and transcription profiles of CD4+ CD8+ thymocytes
Emmanuel AO, et al.
Nature Immunology, 6(3), 1-1 (2018)
TCF12 is mutated in anaplastic oligodendroglioma
Labreche K, et al.
Nature Communications, 6(3), 7207-7207 (2015)
Expression of the bHLH transcription factor Tcf12 (ME1) gene is linked to the expansion of precursor cell populations during neurogenesis
Uittenbogaard M and Chiaramello A
Gene Expression Patterns, 1(2), 115-121 (2002)
Targeted Disruption of TCF12 Reveals HEB as Essential in Human Mesodermal Specification and Hematopoiesis
Li Y, et al.
Stem Cell Reports, 9(3), 779-795 (2017)

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