PRSS56 Antibody
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货号:CSB-PA317372LA01HU
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规格:¥440
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促销:
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图片:
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Western Blot
Positive WB detected in: Rat liver tissue, Rat spleen tissue
All lanes: PRSS56 antibody at 3μg/ml
Secondary
Goat polyclonal to rabbit IgG at 1/50000 dilution
Predicted band size: 65 kDa
Observed band size: 65 kDa -
Immunohistochemistry of paraffin-embedded human eye tissue using CSB-PA317372LA01HU at dilution of 1:100
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其他:
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) PRSS56 Polyclonal antibody
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Uniprot No.:P0CW18
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基因名:PRSS56
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别名:PRSS56 antibody; Serine protease 56 antibody; EC 3.4.21.- antibody
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宿主:Rabbit
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反应种属:Human, Rat
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免疫原:Recombinant Human Serine protease 56 protein (36-116AA)
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
本页面中的产品,PRSS56 Antibody (CSB-PA317372LA01HU),的标记方式是Non-conjugated。对于PRSS56 Antibody,我们还提供其他标记。见下表:
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克隆类型:Polyclonal
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抗体亚型:IgG
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纯化方式:>95%, Protein G purified
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 -
产品提供形式:Liquid
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应用范围:ELISA, WB, IHC
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推荐稀释比:
Application Recommended Dilution WB 1:500-1:5000 IHC 1:20-1:200 -
Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期: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.
相关产品
靶点详情
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功能:Serine protease required during eye development.
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基因功能参考文献:
- 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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相关疾病:Microphthalmia, isolated, 6 (MCOP6)
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蛋白家族:Peptidase S1 family
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组织特异性:Expressed neural retina, cornea, sclera and optic nerve.
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数据库链接:
HGNC: 39433
OMIM: 613517
KEGG: hsa:646960
UniGene: Hs.570310
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