-
- 抗原 See all TMEM237 抗体
- TMEM237 (Transmembrane Protein 237 (TMEM237))
-
抗原表位
- Middle Region
-
适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This TMEM237 antibody is un-conjugated
-
应用范围
- Western Blotting (WB)
- 序列
- AGDQLSNLSN LLQQYKTLAY PFQSLLYLLL ALSTISAFDR IDFAKISVAI
- 交叉反应 （详细）
- Species reactivity (tested):Human
- 纯化方法
- Purified using peptide immunoaffinity column
- 免疫原
- Synthetic peptide directed towards the middle region of human ALS2CR4
- Top Product
- Discover our top product TMEM237 Primary Antibody
-
anti-Transmembrane Protein 237 (TMEM237) (Internal Region) antibody
TMEM237 适用: 人, 小鼠 WB, ELISA, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Transmembrane Protein 237 (TMEM237) (AA 59-78) antibodyTMEM237 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Transmembrane Protein 237 (TMEM237) (AA 251-300) antibodyTMEM237 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Transmembrane Protein 237 (TMEM237) (Middle Region) antibodyTMEM237 适用: 人, 小鼠, Pig, 兔, 大鼠, Cow, 犬, 马 WB 宿主: 兔 Polyclonal unconjugated
-
- 应用备注
- Optimal working dilution should be determined by the investigator.
- 限制
- 仅限研究用
-
- 溶解方式
- Add 50 μL of distilled water to a final concentration of 1 mg/mL.
- 注意事项
- Avoid repeated freezing and thawing.
- 储存条件
- 4 °C/-20 °C
- 储存方法
- Store lyophilized at 2-8 °C or at -20 °C long term. After reconstitution store the antibody undiluted at 2-8 °C for up to one month or in aliquots at -20 °C long term.
-
- 抗原
- TMEM237 (Transmembrane Protein 237 (TMEM237))
- 别名
- ALS2CR4 / TMEM237 (TMEM237 产品)
- 别名
- ALS2CR4 antibody, JBTS14 antibody, Als2cr4 antibody, AI853305 antibody, Gm972 antibody, als2cr4 antibody, als2cr4a antibody, si:dkey-33m14.6 antibody, als2cr4b antibody, sb:cb992 antibody, zgc:101660 antibody, transmembrane protein 237 antibody, transmembrane protein 237a antibody, transmembrane protein 237 L homeolog antibody, transmembrane protein 237b antibody, TMEM237 antibody, Tmem237 antibody, tmem237 antibody, tmem237a antibody, tmem237.L antibody, tmem237b antibody
- 背景
- TMEM237 or ALS2CR4 is a component of the transition zone in primary cilia and required for ciliogenesis. Defects in TMEM237 are the cause of Joubert syndrome type 14 (JBTS14). An autosomal recessive disorder characterized by severe mental retardation, hypotonia, breathing abnormalities in infancy, and dysmorphic facial features. Neuroradiologically, it is characterized by cerebellar vermian hypoplasia/aplasia, thickened and reoriented superior cerebellar peduncles, and an abnormally large interpeduncular fossa, giving the appearance of a molar tooth on transaxial slices (molar tooth sign). Additional variable JBTS14 features include renal disease, abnormal eye movements, and postaxial polydactyly.Synonyms: Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 4 protein, Transmembrane protein 237
- 基因ID
- 65062
- NCBI登录号
- NM_001044385
-
You are here:
