C20orf132 抗体
-
- 抗原 See all C20orf132 products
- C20orf132 (Chromosome 20 Open Reading Frame 132 (C20orf132))
-
适用
- 人, 小鼠, 大鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This C20orf132 antibody is un-conjugated
-
应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C20orf132
- 亚型
- IgG
-
anti-Chromosome 20 Open Reading Frame 132 (C20orf132) (AA 1-608) antibody
C20orf132 适用: 人 WB, IF 宿主: 小鼠 Polyclonal unconjugated
anti-Chromosome 20 Open Reading Frame 132 (C20orf132) (AA 1-275) antibodyC20orf132 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 20 Open Reading Frame 132 (C20orf132) (AA 323-372) antibodyC20orf132 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
-
- 应用备注
-
WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200 - 限制
- 仅限研究用
-
- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: 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
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
-
- 抗原
- C20orf132 (Chromosome 20 Open Reading Frame 132 (C20orf132))
- 别名
- C20orf132 (C20orf132 产品)
- 别名
- C20orf131 antibody, C20orf132 antibody, dJ621N11.3 antibody, dJ621N11.4 antibody, maestro heat like repeat family member 8 antibody, MROH8 antibody
- 背景
-
Synonyms: Uncharacterized protein C20orf132, CT132_HUMAN.
Background: Representing about 2 % of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf132 gene product has been provisionally designated C20orf132 pending further characterization.
- 基因ID
- 140699
-
