C10orf88 抗体 (Cy3)
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- 抗原 See all C10orf88 products
- C10orf88 (Chromosome 10 Open Reading Frame 88 (C10orf88))
- 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 C10orf88 antibody is conjugated to Cy3
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (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 C10orf88
- 亚型
- IgG
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anti-Chromosome 10 Open Reading Frame 88 (C10orf88) (AA 1-445) antibody
C10orf88 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Chromosome 10 Open Reading Frame 88 (C10orf88) (AA 330-379) antibodyC10orf88 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- 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
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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
- -20 °C
- 储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- C10orf88 (Chromosome 10 Open Reading Frame 88 (C10orf88))
- 别名
- C10orf88 (C10orf88 产品)
- 别名
- 3110040E10Rik antibody, AI429544 antibody, chromosome 10 open reading frame 88 antibody, RIKEN cDNA 2310057M21 gene antibody, similar to RIKEN cDNA 2310057M21 antibody, C10orf88 antibody, 2310057M21Rik antibody, RGD1305014 antibody
- 背景
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Synonyms: Chromosome 10 open reading frame 88, CJ088_HUMAN, Em:AC073585.5, FLJ13490, Hypothetical protein LOC80007, Uncharacterized protein C10orf88.
Background: C10orf88 is a 445 amino acid protein encoded by a gene that maps to human chromosome 10q26.13. 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
- 80007
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