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ELK Biotechnology BRCA1 rabbit pAb
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ELK Biotechnology BRCA1 rabbit pAb

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BRCA1 단백질을 인식하는 토끼 폴리클로날 항체로, WB, IHC, IF, ELISA에 사용 가능. 인간 BRCA1 유래 합성 펩타이드로 면역화됨. 핵 및 세포질에 위치하며 DNA 손상 복구 연구에 적합. -20°C에서 1년 보관 가능.

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ELK Biotechnology ES1788-100UL BRCA1 rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES1788-50UL BRCA1 rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology BRCA1 rabbit pAb

제품명

BRCA1 rabbit pAb

제품 정보

항목 내용
Alternative Names BRCA1; RNF53; Breast cancer type 1 susceptibility protein; RING finger protein 53
Applications WB; IHC; IF; ELISA
Recommended Dilutions Western Blot: 1/500 - 1/2000
Immunohistochemistry: 1/100 - 1/300
Immunofluorescence: 1/200 - 1/1000
ELISA: 1/5000
Not yet tested in other applications
Immunogen The antiserum was produced against synthesized peptide derived from human BRCA1 (AA range: 1391–1440)
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Gene ID (Human) 672
Human Swiss-Prot No. P38398
Species Reactivity Human; Rat
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.

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 a large multi-subunit protein complex known as the BRCA1-associated genome surveillance complex (BASC). It associates with RNA polymerase II and interacts with histone deacetylase complexes through the C-terminal domain. This protein plays a role in transcription, 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 subcellular localization and physiological function, producing multiple transcript variants.

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