C22orf28 抗体 (AbBy Fluor® 594)
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- 抗原 See all C22orf28 抗体
- C22orf28 (Chromosome 22 Open Reading Frame 28 (C22orf28))
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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 C22orf28 antibody is conjugated to AbBy 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 HSPC117/C22orf28
- 亚型
- IgG
- Top Product
- Discover our top product C22orf28 Primary Antibody
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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
- C22orf28 (Chromosome 22 Open Reading Frame 28 (C22orf28))
- 别名
- C22orf28 (C22orf28 产品)
- 别名
- C1H22orf28 antibody, C22orf28 antibody, DJ149A16.6 antibody, FAAP antibody, RP1-149A16.6 antibody, c22orf28 antibody, C10H22orf28 antibody, MGC154502 antibody, HSPC117 antibody, AI255213 antibody, AI463255 antibody, RNA 2',3'-cyclic phosphate and 5'-OH ligase antibody, tRNA-splicing ligase RtcB homolog antibody, RTCB antibody, rtcb antibody, rtcb.L antibody, Rtcb antibody
- 背景
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Synonyms: FAAP, Ankyrin repeat domain 54, C22orf28, Chromosome 22 open reading frame 28, DJ149A16.6, HSPC117, Hypothetical protein LOC51493, Novel protein HSPC117, RP1-149A16.6, RTCB_HUMAN, tRNA-splicing ligase RtcB homolog.
Background: HSPC117, also known as C22orf28, is a 505 amino acid protein that is encoded by a gene which maps to human chromosome 22. A highly homologous protein identified in rodents, FAAP (focal adhesion associated protein), encoded by murine D10Wsu52e gene, has been suggested to play a role in regulating cell adhesion dynamics. Chromosome 22 houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. Additionally, 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 leukemias.
- 基因ID
- 51493
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