-
- 抗原 See all TMED6 抗体
- TMED6 (Transmembrane Emp24 Protein Transport Domain Containing 6 (TMED6))
-
抗原表位
- AA 125-153
-
适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This TMED6 antibody is un-conjugated
-
应用范围
- Western Blotting (WB)
- 纯化方法
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- 免疫原
- This TMED6 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 125-153 amino acids from the Central region of human TMED6.
- 亚型
- Ig Fraction
- Top Product
- Discover our top product TMED6 Primary Antibody
-
anti-Transmembrane Emp24 Protein Transport Domain Containing 6 (TMED6) (AA 22-170) antibody
TMED6 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Transmembrane Emp24 Protein Transport Domain Containing 6 (TMED6) (AA 1-240) antibodyTMED6 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
-
- 应用备注
- For WB starting dilution is: 1:1000
- 限制
- 仅限研究用
-
- 状态
- Liquid
- 浓度
- 0.5 mg/mL
- 缓冲液
- Supplied in PBS with 0.09 % (W/V) sodium azide.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
-
- 抗原
- TMED6 (Transmembrane Emp24 Protein Transport Domain Containing 6 (TMED6))
- 别名
- TMED6 (TMED6 产品)
- 别名
- PRO34237 antibody, SPLL9146 antibody, 1810015P03Rik antibody, 1810018I24Rik antibody, transmembrane p24 trafficking protein 6 antibody, TMED6 antibody, Tmed6 antibody
- 背景
- TMED6 (transmembrane emp24 domain-containing protein 6) is a 240 amino acid single-pass type I membrane protein that belongs to the EMP24/GP25L family and contains one GOLD domain. The gene that encodes TMED6 contains around 8,564 bases and maps to human chromosome 16q22.1. Encoding over 900 genes and consisting of approximately 90 million base pairs, chromosome 16 makes up nearly 3 % of the human genome and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, when mutated, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. Alterations in the CREB gene and NOD2 gene, both of which are located on chromosome 16, result in Rubinstein-Taybi syndrome and Crohn's disease, respectively. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
- 分子量
- 28 kDa
- 基因ID
- 146456
- UniProt
- Q8WW62
-
You are here:
