SPATA16 Antibody, FITC conjugated
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中文名稱：SPATA16兔多克隆抗體, FITC偶聯
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貨號：CSB-PA871597LC01HU
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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) SPATA16 Polyclonal antibody
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Uniprot No.：
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基因名：SPATA16
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別名：NYD SP12 antibody; NYD-SP12 antibody; NYDSP12 antibody; SPATA16 antibody; Spermatogenesis associated 16 antibody; Spermatogenesis-associated protein 16 antibody; SPGF6 antibody; SPT16_HUMAN antibody; Testis development protein antibody; Testis development protein NYD-SP12 antibody; Testis specific Golgi protein 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 Spermatogenesis-associated protein 16 protein (238-475AA)
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免疫原種屬：Homo sapiens (Human)
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標記方式：FITC
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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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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：Involved in the formation of sperm acrosome, which implicated its potential role in spermatogenesis and sperm-egg fusion.
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基因功能參考文獻：
- This study demonstrates that Spata16 is indispensable for male fertility in mice, as well as in humans. PMID: 29065458
- Mutation of SPATA16 is associated with globozoospermia. PMID: 27086357
- Case Report: report of a pregnancy obtained in a man with homozygous SPATA16 mutated globozoospermia. PMID: 24825417
- results suggest that NYD-SP12 is involved in spermatogenesis, and that NYD-SP12-encoded protein might function in the Golgi apparatus PMID: 12529416
- study demonstrated NYD-SP12 protein was involved in the formation of the acrosome during spermatogenesis PMID: 16372119
- Results indicate that NYD-SP12 evolves rapidly in both the human and the chimpanzee lineages, which is likely caused by Darwinian positive selection and/or sexual selection. PMID: 17665087
- consanguineous family with three affected brothers, in whom we have identified a homozygous mutation in the spermatogenesis-specific gene SPATA16. This is the first example of a nonsyndromic male infertility condition caused by an autosomal gene defect. PMID: 17847006
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相關疾病：Spermatogenic failure 6 (SPGF6)
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亞細胞定位：Golgi apparatus. Note=Localized to the perinuclear region.
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蛋白家族：SPATA16 family
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組織特異性：Expressed in testis.
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數據庫鏈接：
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