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RPP25L 抗体 (AA 1-100) (Cy5)

This anti-RPP25L antibody is a 兔 多克隆 antibody detecting RPP25L in WB, IF (cc) 和 IF (p). Suitable for 人.
产品编号 ABIN1704727
发货至: 中国

Quick Overview for RPP25L 抗体 (AA 1-100) (Cy5) (ABIN1704727)

抗原

See all RPP25L 抗体
RPP25L (Ribonuclease P/MRP 25 Subunit-Like (RPP25L))

适用

  • 24
  • 9

宿主

  • 24

克隆类型

  • 24
多克隆

标记

  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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This RPP25L antibody is conjugated to Cy5

应用范围

  • 17
  • 12
  • 12
  • 6
  • 3
  • 3
  • 3
  • 2
  • 1
Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 2
    • 1
    AA 1-100

    预测反应

    Human,Mouse,Rat,Dog,Pig,Horse,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human C9orf23

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 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

    RPP25L (Ribonuclease P/MRP 25 Subunit-Like (RPP25L))

    别名

    C9orf23

    背景

    Synonyms: Alba like protein C9orf23, bA296L22.5, C9orf23, MGC29635, Ribonuclease P protein subunit p25 like protein, Ribonuclease P/MRP 25 kDa subunit like, RNase P protein subunit like p25, Rpp25 like protein, RPP25L, RP25L_HUMAN.

    Background: C9orf23 (chromosome 9 open reading frame 23) is a 163 amino acid protein that belongs to the histone-like Alba family and is encoded by a gene that maps to human chromosome 9p13.3. Chromosome 9 consists of about 145 million bases, represents 4 % of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.

    基因ID

    138716
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