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ELK Biotechnology BRCA1 (phospho Ser1524) rabbit pAb
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ELK Biotechnology BRCA1 (phospho Ser1524) rabbit pAb

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BRCA1 인산화(Ser1524) 부위를 인식하는 토끼 폴리클로날 항체로, WB, IHC, IF, ELISA 등에 사용 가능. DNA 손상 반응 및 종양 억제 관련 연구에 적합. 인체, 생쥐, 랫트 시료에 반응. -20°C 보관, 1 mg/ml 농도.

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pk
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ELK Biotechnology ES7268-100UL BRCA1 (phospho Ser1524) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES7268-50UL BRCA1 (phospho Ser1524) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology BRCA1 (phospho Ser1524) rabbit pAb

BRCA1 (phospho Ser1524) rabbit pAb

제품 정보

항목 내용
Product name BRCA1 (phospho Ser1524) rabbit pAb
Alternative Names BRCA1; RNF53; Breast cancer type 1 susceptibility protein; RING finger protein 53
Applications WB; IHC; IF; ELISA
Recommended Dilutions Immunohistochemistry: 1/100 - 1/300
ELISA: 1/10000
Not yet tested in other applications
Immunogen The antiserum was produced against synthesized peptide derived from human BRCA1 around the phosphorylation site of Ser1524. AA range: 1491-1540
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
GeneID (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 a large multi-subunit protein complex known as the BRCA1-associated genome surveillance complex (BASC). This gene product associates with RNA polymerase II and interacts with histone deacetylase complexes through its C-terminal domain. It plays roles in transcription, DNA repair of double-stranded breaks, and recombination. Mutations in this gene are responsible for approximately 40% of inherited breast cancers and over 80% of inherited breast and ovarian cancers. Alternative splicing affects subcellular localization and physiological function, producing many transcript variants.

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