TMED5 抗体 (AA 33-164)
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Quick Overview for TMED5 抗体 (AA 33-164) (ABIN7873987)
抗原
See all TMED5 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 33-164
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原理
- TMED5 Antibody / Transmembrane emp24 domain-containing protein 5
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纯化方法
- Antigen affinity purified
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免疫原
- Recombinant human protein (amino acids D33-K164) was used as the immunogen for the TMED5 antibody.
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亚型
- IgG
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anti-Transmembrane Emp24 Protein Transport Domain Containing 5 (TMED5) (AA 1-229) antibody
TMED5 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Transmembrane Emp24 Protein Transport Domain Containing 5 (TMED5) (AA 33-164) antibodyTMED5 适用: 人, 小鼠, 大鼠 WB, ELISA, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Transmembrane Emp24 Protein Transport Domain Containing 5 (TMED5) (C-Term) antibodyTMED5 适用: 人, 小鼠, 大鼠, Cow, 马, 兔, 犬, 豚鼠, 斑马鱼 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal dilution of the TMED5 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 TMED5 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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- TMED5 (Transmembrane Emp24 Protein Transport Domain Containing 5 (TMED5))
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别名
- TMED5
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背景
- Transmembrane emp24 domain-containing protein 5 is a protein that in humans is encoded by the TMED5 gene. TMED5 is a 229 amino acid single-pass type I membrane protein that belongs to the EMP24/GP25L family and contains one GOLD domain. The gene that encodes TMED5 contains nearly 31,000 bases and maps to human chromosome 1p22.1. As the largest human chromosome, chromosome 1 spans about 260 million base pairs and makes up approximately 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1.
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UniProt
- Q9Y3A6
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途径
- SARS-CoV-2 Protein Interactome
抗原
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