C2orf24 抗体
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- 抗原 See all C2orf24 products
- C2orf24 (Chromosome 2 Open Reading Frame 24 (C2orf24))
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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 C2orf24 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 C2orf24
- 亚型
- IgG
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anti-Chromosome 2 Open Reading Frame 24 (C2orf24) (AA 91-140) antibody
C2orf24 适用: 人, 小鼠, 大鼠, Cow, 豚鼠, 马, 兔, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 2 Open Reading Frame 24 (C2orf24) (N-Term) antibodyC2orf24 适用: 人, 小鼠, 大鼠, Cow, 豚鼠, 马, 兔, 犬, 斑马鱼 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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WB 1:300-5000
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
- C2orf24 (Chromosome 2 Open Reading Frame 24 (C2orf24))
- 别名
- C2orf24 (C2orf24 产品)
- 别名
- c2orf24 antibody, wu:fa05h07 antibody, zgc:55857 antibody, MGC75999 antibody, C12H2orf24 antibody, MGC115028 antibody, DKFZp459J1014 antibody, C2orf24 antibody, CGI-57 antibody, C2H2orf24 antibody, C7H2orf24 antibody, 1810031K17Rik antibody, AU043960 antibody, RGD735175 antibody, cyclin Pas1/PHO80 domain containing 1 antibody, cyclin Pas1/PHO80 domain containing 1 L homeolog antibody, cnppd1 antibody, CNPPD1 antibody, cnppd1.L antibody, Cnppd1 antibody
- 背景
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Synonyms: CDABP0125, CGI 57, chromosome 2 open reading frame 24, CNPD1_HUMAN, CNPPD1, Cyclin Pas1/PHO80 domain-containing protein 1, Protein CNPPD1.
Background: The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The C2orf24 gene product has been provisionally designated C2orf24 pending further characterization.
- 基因ID
- 27013
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