SYCE1 Antibody
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中文名稱：SYCE1兔多克隆抗體
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貨號：CSB-PA022987ESR1HU
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規格：￥440
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圖片：
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Western blot
All lanes: SYCE1 antibody at 3.38μg/ml + Mouse liver tissue
Secondary
Goat polyclonal to rabbit IgG at 1/10000 dilution
Predicted band size: 40, 33, 22 kDa
Observed band size: 40, 58 kDa -
Immunohistochemistry of paraffin-embedded human ovarian cancer using CSB-PA022987ESR1HU at dilution of 1:100 -
Immunohistochemistry of paraffin-embedded human testis tissue using CSB-PA022987ESR1HU at dilution of 1:100
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其他：
產品詳情
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產品名稱：Rabbit anti-Homo sapiens (Human) SYCE1 Polyclonal antibody
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Uniprot No.：
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基因名：SYCE1
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別名：SYCE1 antibody; C10orf94 antibody; Synaptonemal complex central element protein 1 antibody; Cancer/testis antigen 76 antibody; CT76 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：Recombinant Human Synaptonemal complex central element protein 1 protein (132-351AA)
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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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克隆類型：Polyclonal
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抗體亞型：IgG
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純化方式：Antigen Affinity 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：PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
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產品提供形式：Liquid
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應用范圍：ELISA, WB, IHC
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推薦稀釋比：
Application Recommended Dilution WB 1:1000-1:5000 IHC 1:20-1:200 -
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：Major component of the transverse central element of synaptonemal complexes (SCS), formed between homologous chromosomes during meiotic prophase. Requires SYCP1 in order to be incorporated into the central element. May have a role in the synaptonemal complex assembly, stabilization and recombination.
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基因功能參考文獻：
- A mutation in SYCE1 is associated with non-obstructive azoospermia. PMID: 25899990
- Given the known function of the SYCE1 gene, we suggest that the nonsense mutation identified accounts for the primary ovarian insufficiency phenotype. PMID: 25062452
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相關疾病：Premature ovarian failure 12 (POF12); Spermatogenic failure, 15 (SPGF15)
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亞細胞定位：Nucleus. Chromosome.
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蛋白家族：SYCE family
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數據庫鏈接：
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