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Merck
CN

ABE24

Sigma-Aldrich

Anti-BPTF Antibody

from rabbit, purified by affinity chromatography

别名:

Protein Bptf, Bromodomain PHD-finger Transcription Factor

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关于此项目

UNSPSC代码:
12352203
eCl@ss:
32160702
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

纯化方式

affinity chromatography

种属反应性

mouse, human

技术

immunoprecipitation (IP): suitable
western blot: suitable

NCBI登记号

UniProt登记号

运输

wet ice

靶向翻译后修饰

unmodified

基因信息

human ... BPTF(2186)
mouse ... Bptf(207165)

一般描述

Bromodomain PHD finger transcription factor (UniProt: E9Q6A7; also known as Nucleosome-remodeling factor subunit BPTF; Fetal Alz-50 clone 1 protein, Fetal Alzheimer antigen) is encoded by the Bptf (also known as Fac1, Falz) gene (Gene ID: 207165) in murine species. BPTF, SNF2L and pRBAP46/48 are the three subunits of the nucleosome-remodelling factor NURF, an ISWI chromatin-remodeling complex that catalyzes ATP-dependent nucleosome sliding. BPTF mediates NURF target site specificity via interactions with transcription factors, histone variants and histone modifications on transcriptionally active genes. BPTF plays an important role in regulating nucleosome occupancy at nucleosome-free regions (NFRs) at sites occupied by the multivalent factors CTCF and cohesin via direct interaction with CTCF and the cohesin subunit SA2. In addition, BPTF also interacts with c-MYC and plays an essential role in its genomic distribution and biological activity. BPTF is necessary for the survival of c-MYC-overexpressing cells and for c-MYC-driven tumorigenesis in the mouse pancreas. BPTF knockdown leads to decreased c-MYC chromatin accessibility and significantly delays tumour development in pre-neoplastic pancreatic acinar cells. Consistently, BPTF expression in human tumours positively correlates with activation of c-MYC gene signatures.
Target molecular weight ~250 kDa observed. 321.6 kDa calculated. Uncharacterized bands may be observed in some lysate(s).

免疫原

GST-tagged recombinant N-terminal fragment of mouse BPTF.

应用

Anti-BPTF, Cat. No. ABE24, is a rabbit polyclonal antibody that detects BPTF and is tested for use in Western Blotting, Immunocytochemistry, Immunoprecipitation, and Peptide Inhibition Assay.
Evaluated by Western Blotting in NIH/3T3 cell lysate.

Western Blotting Analysis: A 1:2,000 dilution of this antibody detected BPTF in NIH/3T3 cell lysate.

Tested applications

Western Blotting Analysis: A 1:2,000 dilution from a representative lot detected BPTF in MEF-1 and mESC cell lysates.

Immunoprecipitation: A representative lot immunoprecipitated BPTF in Immunoprecipitation application (Qiu, Z., et al. (2015). Mol. Cell. Biol. 35(1):224-237).

Immunocytochemistry Analysis: A 1:500 dilution from a representative lot detected BPTF in A431 cells.

Peptide Inhibition Assay: Target band detection in lysate from NIH/3T3 cells was prevented by pre-blocking of a representative lot with recombinant fragment of mouse BPTF.

Note: Actual optimal working dilutions must be determined by end user as specimens, and experimental conditions may vary with the end user.
Research Category
Epigenetics & Nuclear Function

生化/生理作用

This rabbit polyclonal antibody detects BPTF. It targets an epitope within 103 amino acids from the N-terminal half.

外形

Affinity purified
Purified rabbit polyclonal antibody in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

制备说明

Recommended storage: +2°C to +8°C.

其他说明

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

免责声明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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储存分类代码

12 - Non Combustible Liquids

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Aiman S Alhazmi et al.
The Journal of biological chemistry (2018-08-25)
This article has been withdrawn by Aiman Alhazmi, Marissa Mack, Tiffany Rolle, Jordan Hiegel, Syed Haqqani, Nga Dao, Farheen Zaman, Nak-Kyeong Kim, Neel Scarsdale, Charles Lyons, and Joseph Landry. Some of the genome-wide data sets were flawed and were not analyzed
Nicola Wiechens et al.
PLoS genetics, 12(3), e1005940-e1005940 (2016-03-29)
Within the genomes of metazoans, nucleosomes are highly organised adjacent to the binding sites for a subset of transcription factors. Here we have sought to investigate which chromatin remodelling enzymes are responsible for this. We find that the ATP-dependent chromatin
Ying Li et al.
Nucleic acids research, 44(15), 7173-7188 (2016-05-05)
The modulation of chromatin structure is a key step in transcription regulation in mammalian cells and eventually determines lineage commitment and differentiation. USF1/2, Setd1a and NURF complexes interact to regulate chromatin architecture in erythropoiesis, but the mechanistic basis for this

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