PRSS56 Antibody, Biotin conjugated
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中文名稱：PRSS56兔多克隆抗體, Biotin偶聯
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貨號：CSB-PA317372LD01HU
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規格：￥880
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其他：
產品詳情
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產品名稱：Rabbit anti-Homo sapiens (Human) PRSS56 Polyclonal antibody
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Uniprot No.：
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基因名：PRSS56
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別名：PRSS56 antibody; Serine protease 56 antibody; EC 3.4.21.- antibody
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宿主：Rabbit
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反應種屬：Human
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免疫原：Recombinant Human Serine protease 56 protein (36-116AA)
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免疫原種屬：Homo sapiens (Human)
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標記方式：Biotin
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克隆類型：Polyclonal
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抗體亞型：IgG
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純化方式：>95%, Protein G purified
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濃度：It differs from different batches. Please contact us to confirm it.
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保存緩沖液：Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 -
產品提供形式：Liquid
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應用范圍：ELISA
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Protocols：
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儲存條件：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.
產品評價
相關產品
靶點詳情
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功能：Serine protease required during eye development.
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基因功能參考文獻：
- variations in PRSS56 were evaluated in patients with either primary angle-closure glaucoma (PACG) or high hyperopia. PMID: 24227917
- Idenification of a founder mutation in the PRSS56 gene in Tunisian families with posterior microphthalmia and nanophthalmia. PMID: 23820083
- Corneal diameter decreases with decreasing axial length, suggesting posterior microphthalmos and nanophthalmos represent a spectrum of high hyperopia rather than distinct phenotypes. In the Saudi population PRSS56 mutations are the major cause. PMID: 23127749
- PRSS56 is a good candidate for the causal gene for nanophthalmos in a Mexican-Canadian family cohort. PMID: 21850159
- Together, these data suggest that alterations of this serine protease may contribute to a spectrum of human ocular conditions including reduced ocular size and ACG. PMID: 21532570
- Three different mutations in PRSS56, were detected in microphthalmos patients of the Faroese families. PMID: 21397065
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相關疾病：Microphthalmia, isolated, 6 (MCOP6)
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蛋白家族：Peptidase S1 family
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組織特異性：Expressed neural retina, cornea, sclera and optic nerve.
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數據庫鏈接：
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