SCARF2 Antibody
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中文名稱(chēng):SCARF2兔多克隆抗體
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貨號(hào):CSB-PA042899
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規(guī)格:¥2024
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圖片:
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其他:
產(chǎn)品詳情
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產(chǎn)品名稱(chēng):Rabbit anti-Homo sapiens (Human) SCARF2 Polyclonal antibody
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Uniprot No.:
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基因名:SCARF2
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宿主:Rabbit
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反應(yīng)種屬:Human
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免疫原:Synthesized peptide derived from internal of Human SCARF2.
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免疫原種屬:Homo sapiens (Human)
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克隆類(lèi)型:Polyclonal
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純化方式:The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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濃度:It differs from different batches. Please contact us to confirm it.
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產(chǎn)品提供形式:Liquid
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應(yīng)用范圍:ELISA,IHC
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推薦稀釋比:
Application Recommended Dilution IHC 1:50-1:100 -
Protocols:
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儲(chǔ)存條件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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貨期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
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用途:For Research Use Only. Not for use in diagnostic or therapeutic procedures.
相關(guān)產(chǎn)品
靶點(diǎn)詳情
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功能:Probable adhesion protein, which mediates homophilic and heterophilic interactions. In contrast to SCARF1, it poorly mediates the binding and degradation of acetylated low density lipoprotein (Ac-LDL).
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基因功能參考文獻(xiàn):
- the full VDEGS phenotype may include sclerocornea resulting from homozygosity or compound heterozygosity for loss of function variants in SCARF2. PMID: 24478002
- Mutations in SCARF2 are responsible for Van Den Ende-Gupta syndrome. PMID: 20887961
- SRECII binds to SRECI and has a similar tissue distribution pattern PMID: 12154095
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相關(guān)疾?。?/div>Van den Ende-Gupta syndrome (VDEGS)亞細(xì)胞定位:Membrane; Single-pass type I membrane protein.組織特異性:Predominantly expressed in endothelial cells. Expressed in heart, placenta, lung, kidney, spleen, small intestine and ovary.數(shù)據(jù)庫(kù)鏈接:
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