C22orf9 抗体 (Alexa Fluor 594)
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- 抗原 See all C22orf9 products
- C22orf9 (Chromosome 22 Open Reading Frame 9 (C22orf9))
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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 C22orf9 antibody is conjugated to Alexa Fluor 594
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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 C22orf9
- 亚型
- IgG
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anti-Chromosome 22 Open Reading Frame 9 (C22orf9) (AA 288-337) antibody
C22orf9 适用: 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, Bat, 小鸡, 猴, 非洲爪蟾 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 22 Open Reading Frame 9 (C22orf9) (Middle Region) antibodyC22orf9 适用: 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, 兔 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
- C22orf9 (Chromosome 22 Open Reading Frame 9 (C22orf9))
- 别名
- C22orf9 (C22orf9 产品)
- 别名
- c22orf9 antibody, C22orf9 antibody, AW554572 antibody, mKIAA0930 antibody, KIAA0930 S homeolog antibody, KIAA0930 antibody, RIKEN cDNA 5031439G07 gene antibody, similar to CG9646-PA antibody, KIAA0930 ortholog antibody, kiaa0930.S antibody, KIAA0930 antibody, kiaa0930 antibody, 5031439G07Rik antibody, RGD1304694 antibody, Kiaa0930 antibody
- 背景
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Synonyms: Chromosome 22 open reading frame 9, Hypothetical protein LOC23313, KIAA0930, Uncharacterized protein C22orf9, K0930_HUMAN.
Background: C22orf9 is a 404 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. 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.
- 基因ID
- 23313
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