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ELK Biotechnology PDGFR-α (phospho Tyr754) rabbit pAb
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ELK Biotechnology PDGFR-α (phospho Tyr754) rabbit pAb

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PDGFR-α (phospho Tyr754) rabbit polyclonal antibody로, 인산화된 PDGFR-α 단백질 검출에 적합합니다. WB, IHC, IF, ELISA에 사용 가능하며, 세포막 및 골지체에 위치한 단백질 분석에 활용됩니다. 인간, 생쥐, 랫트 반응성이 있습니다.

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pk
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ELK Biotechnology ES6533-100UL PDGFR-α (phospho Tyr754) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES6533-50UL PDGFR-α (phospho Tyr754) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology PDGFR-α (phospho Tyr754) rabbit pAb

PDGFR-α (phospho Tyr754) rabbit pAb

제품 정보

항목 내용
Product name PDGFR-α (phospho Tyr754) rabbit pAb
Alternative Names PDGFRA; PDGFR2; RHEPDGFRA; Platelet-derived growth factor receptor alpha; PDGF-R-alpha; PDGFR-alpha; Alpha platelet-derived growth factor receptor; Alpha-type platelet-derived growth factor receptor; CD140 antigen-like family member A; CD14
Applications WB; IHC; IF; ELISA
Recommended Dilutions Western Blot: 1/500 - 1/2000
Immunohistochemistry: 1/100 - 1/300
ELISA: 1/5000
Not yet tested in other applications
Immunogen The antiserum was produced against synthesized peptide derived from human PDGFR alpha around the phosphorylation site of Tyr754 (AA range: 721-770)
Host Rabbit
Storage -20°C, 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 122 kDa
Gene ID (Human) 5156
Human Swiss-Prot No. P16234
Cellular Localization Cell membrane; Single-pass type I membrane protein; Cell projection, cilium; Golgi apparatus
Species Reactivity Human; Mouse; Rat

Background

This gene encodes a cell surface tyrosine kinase receptor for members of the platelet-derived growth factor family. These growth factors are mitogens for cells of mesenchymal origin. The identity of the growth factor bound to a receptor monomer determines whether the functional receptor is a homodimer or a heterodimer, composed of both platelet-derived growth factor receptor alpha and beta polypeptides. Studies suggest that this gene plays a role in organ development, wound healing, and tumor progression. Mutations in this gene have been associated with idiopathic hypereosinophilic syndrome, somatic and familial gastrointestinal stromal tumors, and various other cancers.
[Provided by RefSeq, Mar 2012]

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