WFS1 抗体
Quick Overview for WFS1 抗体 (ABIN7232142)
抗原
See all WFS1 抗体适用
宿主
克隆类型
标记
应用范围
-
-
原理
- WFS1 Polyclonal Antibody
-
特异性
- The antibody detects endogenous levels of WFS1 protein
-
纯化方法
- The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen
-
免疫原
- Synthesized peptide derived from part region of human WFS1 protein
-
亚型
- IgG
-
-
anti-Wolfram Syndrome 1 (WFS1) (AA 1-285) antibody
WFS1 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Wolfram Syndrome 1 (WFS1) (Internal Region) antibodyWFS1 适用: 人, 小鼠, 大鼠 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Wolfram Syndrome 1 (WFS1) (AA 791-890) antibodyWFS1 适用: 人 WB, ICC, ELISA, IF (cc), IF (p), IHC (p), IHC (fro) 宿主: 兔 Polyclonal unconjugated
-
-
应用备注
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).
-
说明
-
Primary Antibody
-
限制
- 仅限研究用
-
-
-
状态
- Liquid
-
浓度
- 1 mg/mL
-
缓冲液
- PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.
-
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
- -20 °C
-
储存方法
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
-
-
- WFS1 (Wolfram Syndrome 1 (WFS1))
-
别名
- WFS1
-
背景
- Rabbit Anti-WFS1 Polyclonal Antibody,Wolframin,WFS1 gene encodes a transmembrane protein, which is located primarily in the endoplasmic reticulum and ubiquitously expressed with highest levels in brain, pancreas, heart, and insulinoma beta-cell lines. Mutations in this gene are associated with Wolfram syndrome, also called DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness), an autosomal recessive disorder. The disease affects the brain and central nervous system. Mutations in this gene can also cause autosomal dominant deafness 6 (DFNA6), also known as DFNA14 or DFNA38. Alternatively spliced transcript variants have been found for this gene.,WFS1
-
分子量
- observerd band 97kDa
-
基因ID
- 7466
-
UniProt
- O76024
-
途径
- Sensory Perception of Sound, Carbohydrate Homeostasis, ER-Nucleus Signaling, Negative Regulation of intrinsic apoptotic Signaling, SARS-CoV-2 Protein Interactome
抗原
-
