PGAP2 Antibody
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货号:CSB-PA883397LA01HU
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规格:¥440
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促销:
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图片:
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Immunohistochemistry of paraffin-embedded human brain tissue using CSB-PA883397LA01HU at dilution of 1:100
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Immunohistochemistry of paraffin-embedded human kidney tissue using CSB-PA883397LA01HU at dilution of 1:100
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Immunofluorescent analysis of MCF-7 cells using CSB-PA883397LA01HU at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)
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其他:
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) PGAP2 Polyclonal antibody
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Uniprot No.:Q9UHJ9
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基因名:PGAP2
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别名:PGAP2; FRAG1; Post-GPI attachment to proteins factor 2; FGF receptor-activating protein 1
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宿主:Rabbit
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反应种属:Human
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免疫原:Recombinant Human Post-GPI attachment to proteins factor 2 protein (45-114AA)
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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,PGAP2 Antibody (CSB-PA883397LA01HU),的标记方式是Non-conjugated。对于PGAP2 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, IHC, IF
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推荐稀释比:
Application Recommended Dilution IHC 1:20-1:200 IF 1:50-1:200 -
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.
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靶点详情
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功能:Involved in the lipid remodeling steps of GPI-anchor maturation. Required for stable expression of GPI-anchored proteins at the cell surface.
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基因功能参考文献:
- A Rare Variant in PGAP2 Causes Autosomal Recessive Hyperphosphatasia with Mental Retardation Syndrome, with a Mild Phenotype in Heterozygous Carriers. PMID: 29119105
- Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability. PMID: 23561846
- PGAP2 mutations, affecting the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation syndrome. PMID: 23561847
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相关疾病:Hyperphosphatasia with mental retardation syndrome 3 (HPMRS3)
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亚细胞定位:Golgi apparatus membrane; Multi-pass membrane protein. Endoplasmic reticulum membrane; Multi-pass membrane protein.
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蛋白家族:PGAP2 family
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组织特异性:Ubiquitously expressed, with highest levels in testis and pancreas.
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数据库链接:
HGNC: 17893
OMIM: 614207
KEGG: hsa:27315
STRING: 9606.ENSP00000278243
UniGene: Hs.133968
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