C22orf25 抗体 (AA 25-75) (Biotin)
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- 抗原 See all C22orf25 products
- C22orf25 (Chromosome 22 Open Reading Frame 25 (C22orf25))
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抗原表位
- AA 25-75
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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 C22orf25 antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), 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 C22orf25
- 亚型
- IgG
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anti-Chromosome 22 Open Reading Frame 25 (C22orf25) (N-Term) antibody
C22orf25 适用: 人, 小鼠, 大鼠, 兔, Cow, 犬, Pig, Hamster, 猴, 非洲爪蟾, 小鸡 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 22 Open Reading Frame 25 (C22orf25) (N-Term) antibodyC22orf25 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 22 Open Reading Frame 25 (C22orf25) (N-Term) antibodyC22orf25 适用: 人, 小鼠, 大鼠, 兔, Cow, 犬, 豚鼠, 马, 斑马鱼, 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 - 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 for 12 months.
- 有效期
- 12 months
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- 抗原
- C22orf25 (Chromosome 22 Open Reading Frame 25 (C22orf25))
- 别名
- C22orf25 (C22orf25 产品)
- 别名
- c22orf25 antibody, MGC88919 antibody, C22orf25 antibody, TANGO2 antibody, C17H22orf25 antibody, transport and golgi organization 2 homolog L homeolog antibody, transport and golgi organization 2 homolog antibody, transport and golgi organization 2 homolog (Drosophila) antibody, tango2.L antibody, tango2 antibody, TANGO2 antibody
- 背景
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Synonyms: Uncharacterized protein C22orf25, chromosome 22 open reading frame 25, DKFZp 761 P 1121, Hypothetical protein LOC128989, TNG2_HUMAN, TANGO2, Transport and Golgi organization protein 2 homolog.
Background: Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. The C22orf25 gene product has been provisionally designated C22orf25 pending further characterization.
- 基因ID
- 128989
- UniProt
- Q6ICL3
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