PYROXD1 抗体 (AA 26-453)
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Quick Overview for PYROXD1 抗体 (AA 26-453) (ABIN7873006)
抗原
适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 26-453
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原理
- PYROXD1 Antibody / Pyridine nucleotide-disulfide oxidoreductase domain-containing protein 1
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纯化方法
- Antigen affinity purified
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免疫原
- E. coli-derived recombinant human protein (amino acids A26-N453) was used as the immunogen for the PYROXD1 antibody.
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亚型
- IgG
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anti-Pyridine Nucleotide-Disulphide Oxidoreductase Domain 1 (PYROXD1) (AA 48-230) antibody
PYROXD1 适用: 人, 大鼠, 小鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Pyridine Nucleotide-Disulphide Oxidoreductase Domain 1 (PYROXD1) (N-Term) antibodyVerified PYROXD1 适用: 人 ELISA, IHC, FACS, IF 宿主: 山羊 Polyclonal unconjugated
anti-Pyridine Nucleotide-Disulphide Oxidoreductase Domain 1 (PYROXD1) (AA 24-37) antibodyPYROXD1 适用: 人 WB, ELISA, IHC, IHC (p) 宿主: 山羊 Polyclonal unconjugated
anti-Pyridine Nucleotide-Disulphide Oxidoreductase Domain 1 (PYROXD1) (N-Term) antibodyPYROXD1 适用: 人, 豚鼠, Cow, 马, 兔 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal dilution of the PYROXD1 antibody should be determined by the researcher.
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限制
- 仅限研究用
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状态
- Lyophilized
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缓冲液
- 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
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储存条件
- 4 °C,-20 °C
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储存方法
- After reconstitution, the PYROXD1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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- PYROXD1 (Pyridine Nucleotide-Disulphide Oxidoreductase Domain 1 (PYROXD1))
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别名
- PYROXD1
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背景
- 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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UniProt
- Q8WU10
抗原
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