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C22orf28 抗体 (Cy7)

This anti-C22orf28 antibody is a Rabbit Polyclonal antibody detecting C22orf28 in WB, IF (p). Suitable for Human, Mouse, Rat.
产品编号 ABIN1423652
发货至: 中国

Quick Overview for C22orf28 抗体 (Cy7) (ABIN1423652)

抗原

See all C22orf28 抗体
C22orf28 (Chromosome 22 Open Reading Frame 28 (C22orf28))

适用

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人, 小鼠, 大鼠

宿主

  • 44
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克隆类型

  • 47
多克隆

标记

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This C22orf28 antibody is conjugated to Cy7

应用范围

  • 32
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  • 1
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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
  • 应用备注

    IF(IHC-P) 1:50-200

    限制

    仅限研究用
  • 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
  • 抗原

    C22orf28 (Chromosome 22 Open Reading Frame 28 (C22orf28))

    别名

    C22orf28

    背景

    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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