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Anti-PYROXD1 Antibody

Rabbit IgG polyclonal antibody for PYROXD1 detection. Tested with WB, IHC-P, Direct ELISA in Human;Mouse;Rat.

分类:

一抗 - 多克隆抗体

说明书:

A17214-3

1980元/100ug  

human, mouse, rat

WB,IHC-P,Direct ELISA

Polyclonal

现货

选择规格:

总价格:

---元*1

选择数量:

- +

Product Brief

  • 产品概况

    产品名称Anti-PYROXD1 Antibody
    产品描述Rabbit IgG polyclonal antibody for PYROXD1 detection. Tested with WB, IHC-P, Direct ELISA in Human;Mouse;Rat.
    文献引用格式Anti-PYROXD1 Antibody (Boster Biological Technology, Wuhan, China. Catalog #A17214-3)
    应用范围WB,IHC-P,Direct ELISA
    抗体来源Rabbit
    抗体亚型Rabbit IgG
    推荐配套的二抗和检测试剂Boster recommends Enhanced Chemiluminescent Kit with anti-Rabbit IgG (EK1002) for Western blot, and HRP Conjugated anti-Rabbit IgG Super Vision Assay Kit (SV0002-1) for IHC(P).
    *Blocking peptide 可以联系我们购买。
    免疫原E.coli-derived human PYROXD1 recombinant protein (Position: K48-N230).
    抗体规格100ug/vial

    产品详情

    克隆Polyclonal
    产品形态Lyophilized
    内容Each vial contains 4mg Trehalose, 0.9mg NaCl, 0.2mg Na2HPO4, 0.05mg NaN3.
    *可以提供无载体抗体。
    浓度Add 0.2ml of distilled water will yield a concentration of 500ug/ml.
    储存条件At -20℃ for one year. After reconstitution, at 4℃ for one month. It can also be aliquotted and stored frozen at -20℃ for a longer time. Avoid repeated freezing and thawing.

    指标相关信息 (来源: Uniprot.org)

    小贴士:你可以利用tissue specificity信息来帮助设计阳性和阴性对照。对此有疑问请联系我们技术服务部门。
    基因名PYROXD1
    基因全名pyridine nucleotide-disulphide oxidoreductase domain 1
    Uniprot IDPYROXD1: Q8WU10

    指标背景简介

    Pyridine nucleotide-disulphide oxidoreductase domain 1 is a protein that in humans is encoded by the PYROXD1 gene. It is mapped to 12p12.1. This gene encodes a nuclear-cytoplasmic pyridine nucleotide-disulphide reductase (PNDR). PNDRs are flavoproteins that catalyze the pyridine nucleotide-dependent reduction of thiol residues in other proteins. The encoded protein belongs to the class I pyridine nucleotide-disulphide oxidoreductase family but lacks the C-terminal dimerization domain found in other family members and instead has a C-terminal nitrile reductase domain. It localizes to the nucleus and to striated sarcomeric compartments. Naturally occurring mutations in this gene cause early-onset myopathy with internalized nuclei and myofibrillar disorganization. A pseudogene of this gene has been defined on chromosome 11.

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