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- 抗原 See all DFNB31 抗体
- DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))
- 适用
- 人, 小鼠
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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 DFNB31 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant protein of human WHRN
- 亚型
- IgG
- Top Product
- Discover our top product DFNB31 Primary Antibody
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anti-Deafness, Autosomal Recessive 31 (DFNB31) (AA 808-907) antibody
DFNB31 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 1D9 unconjugated
anti-Deafness, Autosomal Recessive 31 (DFNB31) (AA 808-907) antibodyDFNB31 适用: 人 WB, ELISA, IF 宿主: 小鼠 Monoclonal 2D12 unconjugated
anti-Deafness, Autosomal Recessive 31 (DFNB31) (AA 808-907) antibodyDFNB31 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Deafness, Autosomal Recessive 31 (DFNB31) (AA 708-907) antibodyDFNB31 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Deafness, Autosomal Recessive 31 (DFNB31) (AA 378-406) antibodyDFNB31 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB19059 unconjugated
anti-Deafness, Autosomal Recessive 31 (DFNB31) (AA 385-413), (Middle Region) antibodyDFNB31 适用: 人 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB 1:500 - 1:2000
- 限制
- 仅限研究用
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- 浓度
- 1 mg/mL
- 缓冲液
- Buffer: 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.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))
- 别名
- WHRN (DFNB31 产品)
- 别名
- DFNB31 antibody, CIP98 antibody, PDZD7B antibody, USH2D antibody, WHRN antibody, WI antibody, Cip98 antibody, Whrn antibody, 1110035G07Rik antibody, AW122018 antibody, AW742671 antibody, C430046P22Rik antibody, Dfnb31 antibody, wi antibody, whirlin antibody, WHRN antibody, LOC100555508 antibody, Whrn antibody
- 背景
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Synonyms: Whirlin,Autosomal Recessive Deafness Type 31 Protein,DFNB31,Deafness Autosomal Recessive 31,CASK-Interacting Protein CIP98,KIAA1526,PDZD7B,CIP98,USH2D,WI,WHRN,KIAA1526
Background: This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing results in multiple transcript variants.
- 分子量
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Observed_MW: 110kDa
Calculated_MW: 37kDa/55kDa/59kDa/96kDa
- 基因ID
- 25861
- UniProt
- Q9P202
- 途径
- Sensory Perception of Sound
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