CacheBy
ELK Biotechnology Insulin R (phospho Tyr1361) rabbit pAb
원본

ELK Biotechnology Insulin R (phospho Tyr1361) rabbit pAb

상품 한눈에 보기

인슐린 수용체 인산화 부위(Tyr1361)를 인식하는 토끼 폴리클로날 항체. WB, IHC, IF, ELISA에 사용 가능. 인간, 생쥐, 랫트 반응성. 세포막 및 리소좀 위치 단백질 연구에 적합. -20°C에서 1년 보관.

판매단위
pk
카탈로그 보기

카탈로그

2개 옵션
회원가입 없이 바로 구매하세요
가입하지 않아도 비회원가로 구매하실 수 있습니다.
ELK Biotechnology ES5909-100UL Insulin R (phospho Tyr1361) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES5909-50UL Insulin R (phospho Tyr1361) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology Insulin R (phospho Tyr1361) rabbit pAb

제품명

Insulin R (phospho Tyr1361) rabbit pAb

제품 정보

항목 내용
Alternative Names INSR; Insulin receptor; IR; CD antigen CD220
Applications WB; IHC; IF; ELISA
Recommended Dilutions Western Blot: 1/500 - 1/2000
Immunohistochemistry: 1/100 - 1/300
ELISA: 1/10000
Not yet tested in other applications
Immunogen Synthesized peptide derived from human IR around the phosphorylation site of Tyr1361 (AA range: 1331–1380)
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 95 kDa
Gene ID (Human) 3643
Human Swiss-Prot No P06213
Species Reactivity Human; Mouse; Rat
Cellular Localization Cell membrane; Single-pass type I membrane protein; Late endosome; Lysosome. Binding of insulin to INSR induces internalization and lysosomal degradation of the receptor, down-regulating this signaling pathway after stimulation. In the presence of SORL1, internalized INSR molecules are redirected back to the cell surface, preventing lysosomal catabolism and strengthening insulin signal reception.

Background

This gene encodes a member of the receptor tyrosine kinase family of proteins. The encoded preproprotein is processed to generate alpha and beta subunits forming a heterotetrameric receptor. Binding of insulin or other ligands activates the insulin signaling pathway, regulating glucose uptake and release, as well as carbohydrate, lipid, and protein metabolism. Mutations in this gene cause inherited severe insulin resistance syndromes including type A insulin resistance, Donohue syndrome, and Rabson-Mendenhall syndrome. Alternative splicing results in multiple transcript variants. [RefSeq, Oct 2015]

ELK Biotechnology 상품 둘러보기

전체보기

문의

0

아직 등록된 문의가 없어요.