NME8 Antibody
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中文名稱：NME8兔多克隆抗體
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貨號：CSB-PA025378GA01HU
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規格：￥3,900
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其他：
產品詳情
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Uniprot No.：
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基因名：NME8
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別名：NME8 antibody; SPTRX2 antibody; TXNDC3 antibody; Thioredoxin domain-containing protein 3 antibody; NM23-H8 antibody; NME/NM23 family member 8 antibody; Spermatid-specific thioredoxin-2 antibody; Sptrx-2 antibody
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宿主：Rabbit
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反應種屬：Human,Mouse,Rat
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免疫原：Human TXNDC3
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免疫原種屬：Homo sapiens (Human)
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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, pH 7.3. -20°C, Avoid freeze / thaw cycles.
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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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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：Probably required during the final stages of sperm tail maturation in the testis and/or epididymis, where extensive disulfide bonding of fibrous sheath (FS) proteins occurs. May be involved in the reduction of disulfide bonds within the sperm FS components. In vitro, it has neither NDP kinase nor reducing activity on disulfide bonds.
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基因功能參考文獻：
- Studies suggest that the rs2718058 near gene NME8 on chromosome 7p14.1 might not play a major role in the genetic predisposition to late-onset Alzheimer's disease (LOAD) in the North Han Chinese. PMID: 27144521
- Addition of the minor allele for rs670139 (MS4A4E), rs9331896 (CLU), and rs12155159 (NME8) was nominally associated with change on the DWRT, DSST, and WFT, respectively, in whites. PMID: 27781389
- NME8 locus polymorphism is associated with cognitive decline, cerebrospinal fluid and neuroimaging biomarkers in Alzheimer's disease. PMID: 25486118
- GPR141-NME8 locus had strong genetic effect on the susceptibility to generalized periodontitis in Japanese individuals with history of smoking. identified 2 suggestive loci for periodontitis in a Japanese population. PMID: 25672891
- Our approach yielded 26 candidate genes differentially expressed between patients (Osteoarthritis) and controls. The presence of allelic imbalances confirms cis-regulatory mechanisms for RHOB and TXNDC3. PMID: 16642435
- genetic association of RHOB and TXNDC3 with osteoarthritis was detected PMID: 17304710
- Primary ciliary dyskinesia is caused by an SNP-induced modification of the ratio of two physiological isoforms of TXNDC3 generated by alternative splicing. PMID: 17360648
- The minor allele frequencies of TXNDC3 in East Asian individuals are significantly different from those in United Kingdom control individuals. PMID: 18471322
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相關疾病：Ciliary dyskinesia, primary, 6 (CILD6)
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亞細胞定位：Cytoplasm.
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蛋白家族：NDK family
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組織特異性：Testis-specific. Expressed only in primary spermatocytes and round spermatids.
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數據庫鏈接：
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