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ELK Biotechnology CD36 rabbit pAb
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ELK Biotechnology CD36 rabbit pAb

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CD36 단백질을 인식하는 토끼 폴리클로날 항체로, WB, IHC, ELISA에 사용 가능. 세포막 단백질 검출에 적합하며, 인간, 마우스, 랫트, 틸라피아 시료에 반응. 합성 펩타이드 면역원으로 제작되어 높은 특이성과 신뢰성 제공.

카탈로그번호
ES4315-xxxxx (2개 옵션)
판매단위
pk
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2개 옵션
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ELK Biotechnology ES4315-100UL CD36 rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES4315-50UL CD36 rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology CD36 rabbit pAb

제품명

CD36 rabbit pAb

제품 정보

항목 내용
Alternative Names CD36; GP3B; GP4; Platelet glycoprotein 4; Fatty acid translocase; FAT; Glycoprotein IIIb; GPIIIB; Leukocyte differentiation antigen CD36; PAS IV; PAS-4; Platelet collagen receptor; Platelet glycoprotein IV; GPIV; Thrombospondin receptor; CD36
Applications WB; IHC; 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 the internal region of human CD36 (AA range: 331–380)
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 90 kDa
Gene ID (Human) 948
Human Swiss-Prot No. P16671
Cellular Localization Cell membrane; Multi-pass membrane protein; Membrane raft; Golgi apparatus; Apical cell membrane. Upon ligand-binding, internalized through dynamin-dependent endocytosis.
Species Reactivity Human; Mouse; Rat; Tilapia

Background

The protein encoded by this gene is the fourth major glycoprotein of the platelet surface and serves as a receptor for thrombospondin in platelets and various cell lines. Since thrombospondins are widely distributed proteins involved in a variety of adhesive processes, this protein may have important functions as a cell adhesion molecule. It binds to collagen, thrombospondin, anionic phospholipids, and oxidized LDL. It directly mediates cytoadherence of Plasmodium falciparum parasitized erythrocytes and binds long-chain fatty acids, functioning in their transport and/or regulation. Mutations in this gene cause platelet glycoprotein deficiency. Multiple alternatively spliced transcript variants have been identified for this gene (RefSeq, Feb 2014).

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