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- 抗原 See all WFS1 抗体
- WFS1 (Wolfram Syndrome 1 (WFS1))
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抗原表位
- AA 1-285
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This WFS1 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (IF)
- 序列
- MDSNTAPLGP SCPQPPPAPQ PQARSRLNAT ASLEQERSER PRAPGPQAGP GPGVRDAAAP AEPQAQHTRS RERADGTGPT KGDMEIPFEE VLERAKAGDP KAQTEVGKHY LQLAGDTDEE LNSCTAVDWL VLAAKQGRRE AVKLLRRCLA DRRGITSENE REVRQLSSET DLERAVRKAA LVMYWKLNPK KKKQVAVAEL LENVGQVNEH DGGAQPGPVP KSLQKQRRML ERLVSSESKN YIALDDFVEI TKKYAKGVIP SSLFLQDDED DDELAGKSPE DLPLR
- 交叉反应
- 人, 小鼠
- 产品特性
- Polyclonal Antibodies
- 免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-285 of human WFS1 (NP_001139325.1).
- 亚型
- IgG
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anti-Wolfram Syndrome 1 (WFS1) (Internal Region) antibody
WFS1 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, ELISA, IF (cc), IF (p), IHC (p), IHC (fro), ICC 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB,1:500 - 1:2000,IF,1:50 - 1:200
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- 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.
- 注意事项
- Avoid freeze / thaw cycles
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- WFS1 (Wolfram Syndrome 1 (WFS1))
- 别名
- WFS1 (WFS1 产品)
- 别名
- WFRS antibody, WFS antibody, WFSL antibody, CG4917 antibody, Dmel\\CG4917 antibody, GB15257 antibody, WFS1 antibody, AI481085 antibody, wolframin antibody, wfs1 antibody, wolframin ER transmembrane glycoprotein antibody, wolfram syndrome 1 antibody, wolframin antibody, Wolfram syndrome 1 (wolframin) L homeolog antibody, Wfs1 antibody, WFS1 antibody, wfs1 antibody, LOC552818 antibody, CpipJ_CPIJ013087 antibody, wfs1.L antibody
- 背景
- This 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,CTRCT41,WFRS,WFS,WFSL,wolframin,Cancer,Signal Transduction,Cell Biology & Developmental Biology,Growth factor,Insulin and insulin-like,Endocrine & Metabolism,Endocrine and metabolic diseases,Metabolic disorders,Neuroscience,WFS1
- 分子量
- 100 kDa
- 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
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