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Thermo Fisher Scientific BRCA1 Monoclonal Antibody (17F8)
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Thermo Fisher Scientific BRCA1 Monoclonal Antibody (17F8)

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BRCA1 단백질을 인식하는 Mouse Monoclonal Antibody (Clone 17F8). Western blot, IHC, ICC, ELISA, IP, ChIP 등에 사용 가능. Human 및 Mouse 반응성. Protein G 정제, PBS 용액 형태로 제공되며, 장기 보관 시 -20°C 권장.

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MA123160
판매단위
pk
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마지막 업데이트 2025. 08. 03. 오전 11:56
Thermo Fisher Scientific MA123160 BRCA1 Monoclonal Antibody (17F8) 100 ul pk판매 단위 pk ·
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706,800원VAT 포함 777,480원

Thermo Fisher Scientific · Thermo Fisher Scientific BRCA1 Monoclonal Antibody (17F8)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:3,000
Immunohistochemistry (Paraffin) (IHC (P)) Assay-dependent
Immunocytochemistry (ICC/IF) 1 µg/mL
ELISA Assay-dependent
Immunoprecipitation (IP) Assay-dependent
ChIP assay (ChIP) Assay-dependent

Product Specifications

Specification Description
Species Reactivity Human, Mouse
Published Species Human
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone 17F8
Immunogen Protein fragment expressed in E. coli corresponding to amino acids 762–1315 of BRCA1
Conjugate Unconjugated
Form Liquid
Concentration 1.55 mg/mL
Purification Protein G
Storage Buffer PBS
Contains No preservative
Storage Conditions Store at 4°C short term; for long term, store at -20°C avoiding freeze/thaw cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_557804

Product Specific Information

  • Recommended positive controls: 293T, A431, HeLa
  • This antibody does not recognize the delta exon 11 splice variant of BRCA1
  • The antigen used to produce MA1-23160 has a predicted molecular weight of ~208 kDa

Target Information

BRCA1 (Breast and Ovarian Cancer Susceptibility Protein 1) is a nuclear phosphoprotein involved in maintaining genomic stability and acting as a tumor suppressor. It forms part of the BASC (BRCA1-associated genome surveillance complex) and interacts with RNA polymerase II and histone deacetylase complexes. BRCA1 plays a role in transcription, DNA repair of double-stranded breaks, and recombination. Mutations in BRCA1 are responsible for approximately 40% of inherited breast cancers and over 80% of inherited breast and ovarian cancers. Alternative splicing affects the localization and function of this gene, and several disease-associated variants have been described.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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