IdnK 抗体 (AA 56-182)
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北京 101111
Quick Overview for IdnK 抗体 (AA 56-182) (ABIN7602035)
抗原
See all IdnK (IDNK) 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 56-182
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原理
- Anti-IDNK Antibody
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产品特性
- Anti-IDNK Antibody (ABIN7602035). Tested in WB, ELISA applications. This antibody reacts with Human, Mouse, Rat. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.
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纯化方法
- Immunogen affinity purified.
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免疫原
- E.coli-derived human IDNK recombinant protein (Position: Q56-E182). Human IDNK shares 70.9% amino acid (aa) sequence identity with both mouse and rat IDNK.
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亚型
- IgG
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anti-IdnK Gluconokinase Homolog (IDNK) (AA 41-141) antibody
IDNK 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 3B7 unconjugated
anti-IdnK Gluconokinase Homolog (IDNK) (AA 41-141) antibodyIDNK 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 1H4 unconjugated
anti-IdnK Gluconokinase Homolog (IDNK) (AA 11-45) antibodyIDNK 适用: 人 WB 宿主: 兔 Polyclonal RB54309 unconjugated
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应用备注
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Western blot, 0.1-0.25 μg/mL, Human, Mouse, Rat
ELISA, 0.1-0.5 μg/mL, -
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限制
- 仅限研究用
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状态
- Lyophilized
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溶解方式
- Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
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浓度
- 500 μg/mL
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缓冲液
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
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储存条件
- 4 °C,-20 °C
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储存方法
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At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
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- IdnK (IDNK) (IdnK Gluconokinase Homolog (IDNK))
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别名
- IDNK
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背景
- C9orf103 (chromosome 9 open reading frame 103), also known as gluconate kinase, is a 187 amino acid protein that belongs to the gluconokinase gntK/gntV family and catalyzes the conversion of ATP and D-gluconate to ADP and 6-D-gluconate. Existing as three alternatively spliced isoforms, the gene encoding C9orf103 maps to human chromosome 9q21.32. Chromosome 9 consists of about 145 million bases, represents 4?% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster.
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分子量
- 21 kDa
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基因ID
- 414328
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UniProt
- Q5T6J7
抗原
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