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CXorf21 抗体 (AA 165-215) (Cy3)

This Cy3-conjugated 兔 多克隆 anti-CXorf21 antibody specifically detects CXorf21 in WB, FACS 和 IF (p). The antibody is reactive with 人, 小鼠 和 大鼠 samples.
产品编号 ABIN1421249
发货至: 中国
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Quick Overview for CXorf21 抗体 (AA 165-215) (Cy3) (ABIN1421249)

抗原

CXorf21 (Chromosome X Open Reading Frame 21 (CXorf21))

适用

人, 小鼠, 大鼠

宿主

  • 21
  • 2

克隆类型

  • 22
  • 1
多克隆

标记

  • 5
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CXorf21 antibody is conjugated to Cy3

应用范围

  • 18
  • 14
  • 12
  • 5
  • 3
  • 2
  • 1
Western Blotting (WB), Flow Cytometry (FACS), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 15
    • 8
    AA 165-215

    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 CXorf21

    亚型

    IgG
  • 应用备注

    FCM 1:20-100
    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

    CXorf21 (Chromosome X Open Reading Frame 21 (CXorf21))

    别名

    CXorf21

    背景

    Synonyms: Chromosome X open reading frame 21, FLJ11577, Hypothetical protein LOC80231, Uncharacterized protein CXorf21, CX021_HUMAN.

    Background: The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. The CXorf21 gene product has been provisionally designated CXorf21 pending further characterization.

    基因ID

    80231

    UniProt

    Q9HAI6
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