PIH1D3 Antibody, Biotin conjugated
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中文名稱：PIH1D3兔多克隆抗體, Biotin偶聯
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貨號：CSB-PA878855LD01HU
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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) PIH1D3 Polyclonal antibody
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Uniprot No.：
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基因名：PIH1D3
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別名：PIH1D3 antibody; CXorf41 antibody; Protein PIH1D3 antibody; PIH1 domain-containing protein 3 antibody; Sarcoma antigen NY-SAR-97 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 Protein PIH1D3 protein (1-214AA)
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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：Plays a role in cytoplasmic pre-assembly of axonemal dynein.
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基因功能參考文獻：
- Study propose that PIH1D3 is part of a complementary conserved R2TP-like HSP90 co-chaperone complex, the loss of which affects assembly of a subset of inner arm dyneins. PMID: 28176794
- Mutations in PIH1D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm Defects PMID: 28041644
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相關疾病：Ciliary dyskinesia, primary, 36, X-linked (CILD36)
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亞細胞定位：Cytoplasm. Golgi apparatus, trans-Golgi network.
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蛋白家族：PIH1 family
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組織特異性：Expressed in testis, small intestine, prostate, adrenal gland, spleen, lung, bladder, breast and ovary. Expressed in ciliated epithelial cells.
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數據庫鏈接：
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