TSPYL1 Antibody
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中文名稱：TSPYL1兔多克隆抗體
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貨號：CSB-PA065090
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規格：￥1100
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圖片：
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Gel: 8%SDS-PAGE,Lysate: 40 μg,Lane 1-2: Mouse brain tissue, Mouse heart tissue,Primary antibody: CSB-PA065090(TSPYL1 Antibody) at dilution 1/200 dilution,Secondary antibody: Goat anti rabbit IgG at 1/8000 dilution,Exposure time: 2 minutes
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其他：
產品詳情
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Uniprot No.：
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基因名：TSPYL1
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別名：SIDDT antibody; Testis specific like protein Y encoded antibody; Testis specific Y encoded like protein 1 antibody; Testis-specific Y-encoded-like protein 1 antibody; TSPY like antibody; TSPY like 1 antibody; TSPY like protein 1 antibody; TSPY-like protein 1 antibody; TSPYL antibody; TSPYL1 antibody; TSYL1_HUMAN antibody
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宿主：Rabbit
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反應種屬：Human,Mouse
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免疫原：Synthetic peptide of Human TSPYL1
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免疫原種屬：Homo sapiens (Human)
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標記方式：Non-conjugated
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抗體亞型：IgG
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純化方式：Antigen affinity purification
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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：-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
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產品提供形式：Liquid
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應用范圍：ELISA,WB
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推薦稀釋比：
Application Recommended Dilution ELISA 1:2000-1:5000 WB 1:500-1:2000 -
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
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靶點詳情
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基因功能參考文獻：
- Results show that mutations and polymorphisms in the TSPYL1 gene were not associated with sudden infant death syndrome in a cohort of 165 deceased Swiss infants. PMID: 25449952
- Mutations in the TSPYL1 gene do not seem to play a major role in the pathogenesis of idiopathic male infertility, and mutation screening of the TSPYL1 gene can currently not be recommended in routine diagnostics of idiopathic male infertility. PMID: 22137496
- The chromatin remodeling factor TSPYL1 had a very similar pattern of expression with an incremental increase in HPFH and decreased expression in deltabeta-thalassemia. PMID: 16952470
- Mutations in TSPYL1 may contribute to anomalies of testicular development/function. PMID: 19463995
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相關疾病：Sudden infant death with dysgenesis of the testes syndrome (SIDDT)
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亞細胞定位：Nucleus, nucleolus.
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蛋白家族：Nucleosome assembly protein (NAP) family
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組織特異性：Expressed in testis, ovary, liver, spleen, brain, kidney, prostate, lung, liver, and heart.
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數據庫鏈接：
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