C2orf68 抗体
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- 抗原 See all C2orf68 products
- C2orf68 (Chromosome 2 Open Reading Frame 68 (C2orf68))
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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 C2orf68 antibody is un-conjugated
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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 C2orf68
- 亚型
- IgG
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anti-Chromosome 2 Open Reading Frame 68 (C2orf68) (AA 51-100) antibody
C2orf68 适用: 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, 兔, Hamster, 猴, Pig 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
- C2orf68 (Chromosome 2 Open Reading Frame 68 (C2orf68))
- 别名
- C2orf68 (C2orf68 产品)
- 别名
- HCRCN81 antibody, 1500031N04Rik antibody, 2810411C16Rik antibody, AI461894 antibody, chromosome 2 open reading frame 68 antibody, chromosome 13 open reading frame, human C2orf68 antibody, chromosome 2 open reading frame 68 L homeolog antibody, RIKEN cDNA 0610030E20 gene antibody, chromosome 11 open reading frame, human C2orf68 antibody, C2orf68 antibody, C13H2orf68 antibody, c2orf68.L antibody, 0610030E20Rik antibody, C11H2orf68 antibody
- 背景
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Synonyms: Chromosome 2 open reading frame 68, FLJ14112, FLJ35653, MGC131675, CB068_HUMAN.
Background: C2orf68, also known as FLJ14112, FLJ35653 or MGC131675, is a 168 amino acid protein belonging to the UPF0561 family. Existing as two alternatively spliced isoforms, C2orf68 is encoded by a gene that maps to human chromosome 2q11.2. As the second largest human chromosome, chromosome 2 makes up approximately 8 % of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare 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 related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.
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