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ELK Biotechnology BRCA1 (phospho Ser1457) rabbit pAb
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ELK Biotechnology BRCA1 (phospho Ser1457) rabbit pAb

상품 한눈에 보기

BRCA1 단백질의 Ser1457 인산화 부위를 인식하는 rabbit polyclonal 항체. WB 및 ELISA에 적합하며, 인간, 랫드, 마우스에 반응. 핵 및 세포질에서 DNA 손상 반응 연구에 활용 가능. -20°C에서 1년 보관.

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pk
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ELK Biotechnology ES7269-100UL BRCA1 (phospho Ser1457) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES7269-50UL BRCA1 (phospho Ser1457) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology BRCA1 (phospho Ser1457) rabbit pAb

BRCA1 (phospho Ser1457) rabbit pAb

제품 개요

BRCA1 단백질의 Ser1457 인산화 부위를 특이적으로 인식하는 rabbit polyclonal 항체입니다. DNA 손상 복구 및 종양 억제 기전 연구에 유용하며, Western blot 및 ELISA 분석에 적합합니다.

제품 정보

항목 내용
Product name BRCA1 (phospho Ser1457) rabbit pAb
Alternative Names BRCA1; RNF53; Breast cancer type 1 susceptibility protein; RING finger protein 53
Applications WB; ELISA
Recommended Dilutions Western Blot: 1/500 - 1/2000
ELISA: 1/5000
Not yet tested in other applications
Immunogen The antiserum was produced against synthesized peptide derived from human BRCA1 around the phosphorylation site of Ser1457 (AA range: 1423–1472)
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 180 kD
Gene ID (Human) 672
Human Swiss-Prot No. P38398
Cellular Localization Nucleus, Chromosome, Cytoplasm. Localizes at sites of DNA damage at double-strand breaks (DSBs); recruitment to DNA damage sites is mediated by ABRAXAS1 and the BRCA1-A complex (PubMed:26778126). Translocated to the cytoplasm during UV-induced apoptosis (PubMed:20160719). Isoform 3: Cytoplasm; Isoform 5: Cytoplasm.
Species Reactivity Human; Rat; Mouse

Background

This gene encodes a nuclear phosphoprotein that plays a role in maintaining genomic stability and acts as a tumor suppressor. The encoded protein combines with other tumor suppressors, DNA damage sensors, and signal transducers to form the BRCA1-associated genome surveillance complex (BASC). It associates with RNA polymerase II and histone deacetylase complexes, contributing to transcription regulation, DNA repair of double-stranded breaks, and recombination. Mutations in this gene are responsible for approximately 40% of inherited breast cancers and more than 80% of inherited breast and ovarian cancers. Alternative splicing modulates its subcellular localization and physiological function.

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