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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
Protein fragment expressed in E. coli corresponding to amino acids 762-1315.
- 亚型:
IgG1
- 形态:
Liquid
- 保存条件:
Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
- 克隆性:
Monoclonal
- 标记物:
Unconjugated
- 适应物种:
Human, Mouse
- 保质期:
12 months from the shipping date of the product.
- 抗原来源:
Human
- 目录编号:
GTX70111
- 级别:
Primary Antibodies
- 库存:
Available
- 供应商:
GeneTex
- 宿主:
Mouse
- 应用范围:
WB, ICC/IF, IHC-P, IP, ELISA, ChIP assay, IHC
- 浓度:
1.55 mg/ml (Please refer to the vial label for the specific concentration.)
- 靶点:
This antibody does not recognize the delta exon 11 splice variant of BRCA1. In a high proportion of breast and ovarian cancer cell lines, BRCA1 aberrantly mislocates to the cytoplasm.
- 抗体英文名:
BRCA1 antibody [17F8] - ChIP grade
- 抗体名:
BRCA1 抗体 [17F8] - ChIP grade
- 规格:
100 μl
BRCA1 antibody 6B4 (GTX70115) and BRCA1 antibody 17F8 (GTX70111) were used for ChIP assay.
The 6B4 and 17F8 mixture (3 microgram each), or normal mouse IgG (6 microgram) were incubated with HeLa chromatin extract (100 umicrogram each) in the ChIP assay.
Enrichment of genomic DNA on a BRCA1 target gene promoter (HMGA2) was validated by a Q-PCR assay.
BRCA1 antibody 6B4 (GTX70115) and BRCA1 antibody 17F8 (GTX70111) was used for IP-WB assay.
6B4 alone (4 microgram), 17F8 alone (4 microgram), 6B4 plus 17F8 (2 microgram each), and mouse control normal IgG were used in an immunoprecipitation assay with MCF7 cell extract.
Immunoprecipitated BRCA1 was detected in WB using BRCA1 antibody 6B4 at 1:1000 dilution.
Non-transfected (–) and transfected (+) 293T whole cell extracts (60 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with BRCA1 antibody [17F8] - ChIP grade (GTX70111) diluted at 1:500. The HRP-conjugated anti-mouse IgG antibody (GTX213111-01) was used to detect the primary antibody.
Wild-type (WT) and BRCA1 knockout (KO) HeLa cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with BRCA1 antibody [17F8] - ChIP grade (GTX70111) diluted at 1:500. The HRP-conjugated anti-mouse IgG antibody (GTX213111-01) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.
BRCA1 antibody [17F8] - ChIP grade detects BRCA1 protein by western blot analysis. Various whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and blotted with BRCA1 antibody [17F8] - ChIP grade (GTX70111) diluted by 1:500. The HRP-conjugated anti-mouse IgG antibody (GTX213111-01) was used to detect the primary antibody.
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文献和实验Lu M et al., Oncogene 2000 (PMID:11175350)
de Toledo SM et al., Oncogene 2000 (PMID:11175332)
Arizti P et al., Mol Cell Biol 2000 (PMID:11003642)
Sun X et al., Nucleic Acids Res 2020 (PMID:32729622)
Huang AC et al., Anticancer Res 2019 (PMID:30952724)
Iqbal J et al., PLoS Pathog 2016 (PMID:27764250)
Alcaraz Silva B et al., DNA Repair (Amst) 2016 (PMID:27842255)
Johnson BA et al., Virology 2016 (PMID:27770701)
Shih YL et al., Oncol Rep 2016 (PMID:27572101)
Urban V et al., J Cell Biol 2016 (PMID:27502483)
Shang HS et al., Oncol Rep 2016 (PMID:27499229)
Dutta D et al., PLoS Pathog 2015 (PMID:26121674)
Buisson R et al., Nucleic Acids Res 2012 (PMID:22941656)
Wada O et al., Oncogene 2004 (PMID:15208681)
Bernard-Gallon DJ et al., Anticancer Res 2004 (PMID:15015615)
Altiok S et al., J Biol Chem 1999 (PMID:10542266)
Bernard-Gallon DJ et al., Int J Cancer 1999 (PMID:10417779)
Yoshikawa K et al., Clin Cancer Res 1999 (PMID:10389907)
Bernard-Gallon DJ et al., Int J Cancer 1999 (PMID:10328242)
Bosviel R et al., OMICS 2012 (PMID:22339411)
Vardi A et al., In Vivo 2010 (PMID:20668305)
Oishi H et al., J Biol Chem 2006 (PMID:16260778)
Ongusaha PP et al., Oncogene 2003 (PMID:12802282)
Bernard-Gallon DJ et al., Breast Cancer Res 2001 (PMID:11250747)
Herring Sperm DNA37% Formaldehyde (ACS reagent grade)1.25 M glycineProtocol: (Generalized for all cell types- inquire for details regarding particular cell types) For all the following steps,use the pipets that are specifically designated for ChIP use
Characterization and Quality Control of Antibodies Used in ChIP Assays
, modifying enzymes, and chromatin-interacting proteins. The final purpose of the characterization and QC is to label antibodies as chromatin immunoprecipitation (ChIP) grade. Indeed, the ChIP method is extensively used in epigenetics to study gene regulation
ChIP‐chip for Genome‐Wide Analysis of Protein Binding in Mammalian Cells
Abstract Table of Contents Materials Figures Literature Cited Abstract ChIP?chip combines
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