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ELK Biotechnology PDGFR-β rabbit pAb
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ELK Biotechnology PDGFR-β rabbit pAb

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PDGFR-β 단백질을 인식하는 토끼 폴리클로날 항체로, WB, IHC, IF, ELISA에 사용 가능. 인간, 마우스, 랫트 반응성. 세포막 및 세포질 소기관에 위치한 PDGFR-β 검출에 적합. -20°C에서 1년 보관 가능.

판매단위
pk
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ELK Biotechnology ES6545-100UL PDGFR-β rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES6545-50UL PDGFR-β rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology PDGFR-β rabbit pAb

ELK Biotechnology PDGFR-β rabbit pAb

제품 설명

PDGFR-β rabbit pAb는 혈소판 유래 성장 인자 수용체 베타(Platelet-derived growth factor receptor beta, PDGFR-β)를 인식하는 폴리클로날 항체입니다. 본 항체는 인간 PDGFR-β에서 유래한 합성 펩타이드(AA 991–1040)에 대해 생성되었으며, 다양한 종(인간, 마우스, 랫트)에 반응합니다.

제품 스펙

항목 내용
Product name PDGFR-β rabbit pAb
Alternative Names PDGFRB; PDGFR; PDGFR1; Platelet-derived growth factor receptor beta; PDGF-R-beta; PDGFR-beta; Beta platelet-derived growth factor receptor; Beta-type platelet-derived growth factor receptor; CD140 antigen-like family member B
Applications WB; IHC; IF; ELISA
Recommended Dilutions WB: 1/500–1/2000
IHC: 1/100–1/300
IF: 1/200–1/1000
ELISA: 1/5000
(Other applications not yet tested)
Immunogen Synthesized peptide derived from human PDGFR beta (AA range: 991–1040)
Species Reactivity Human; Mouse; Rat
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 135–180 kDa
Gene ID (Human) 5159
Human Swiss-Prot No. P09619
Cellular Localization Cell membrane; Single-pass type I membrane protein; Cytoplasmic vesicle; Lysosome lumen. After ligand binding, the autophosphorylated receptor is ubiquitinated and internalized, leading to its degradation.
Storage -20°C, 1 year
Host Rabbit

Background

This gene encodes a cell surface tyrosine kinase receptor for members of the platelet-derived growth factor family. These growth factors act as mitogens for cells of mesenchymal origin. The receptor can form homodimers or heterodimers depending on the ligand bound. The gene is located on chromosome 5 near GM-CSF and M-CSF receptor genes, which may be implicated in the 5-q syndrome. A translocation between chromosomes 5 and 12 that fuses this gene with ETV6 can result in chronic myeloproliferative disorder with eosinophilia. (RefSeq, Jul 2008)

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