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- 抗原 See all C10orf93 (TTC40) products
- C10orf93 (TTC40) (Tetratricopeptide Repeat Domain 40 (TTC40))
- 适用
- 人, 小鼠, 大鼠
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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 C10orf93 antibody is un-conjugated
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应用范围
- 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 C10orf93
- 亚型
- IgG
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- 应用备注
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IHC-P 1:200-400
IF(IHC-P) 1:50-200 - 限制
- 仅限研究用
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- 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
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- 抗原
- C10orf93 (TTC40) (Tetratricopeptide Repeat Domain 40 (TTC40))
- 别名
- C10orf93 (TTC40 产品)
- 别名
- C10orf123 antibody, C10orf124 antibody, C10orf92 antibody, C10orf93 antibody, RP13-137A17.3 antibody, bA288G11.4 antibody, bA288G11.5 antibody, bB137A17.2 antibody, bB137A17.3 antibody, cilia and flagella associated protein 46 antibody, CFAP46 antibody
- 背景
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Synonyms: TTC40, C10orf92, C10orf93, C10orf123, C10orf124, bA288G11.4, bA288G11.5, bB137A17.2, bB137A17.3, Protein CFAP46, Cilia- and flagella-associated protein 46, Tetratricopeptide repeat protein 40, CFAP46
Background: C10orf93 , also known as C10orf124 or TPR repeat-containing protein C10orf93, is a 1,530 amino acid protein that contains two TPR repeats and exists as three alternatively spliced isoforms. The gene encoding C10orf93 maps to human chromosome 10q26.3. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5 % of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman?s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
- 基因ID
- 54777
- UniProt
- Q8IYW2
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