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CNTD2 抗体 (Cy7)

CNTD2 适用: 人 IF (p) 宿主: 兔 Polyclonal Cy7
产品编号 ABIN1422260
发货至: 中国
  • 抗原 See all CNTD2 products
    CNTD2 (Cyclin N-terminal Domain Containing 2 (CNTD2))
    适用
    • 20
    • 1
    • 1
    • 1
    • 1
    • 1
    宿主
    • 20
    克隆类型
    • 20
    多克隆
    标记
    • 7
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
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    This CNTD2 antibody is conjugated to Cy7
    应用范围
    • 12
    • 5
    • 3
    • 2
    • 2
    • 1
    Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    交叉反应
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human CNTD2
    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
    CNTD2 (Cyclin N-terminal Domain Containing 2 (CNTD2))
    别名
    CNTD2 (CNTD2 产品)
    别名
    MGC145598 antibody, cyclin N-terminal domain containing 2 antibody, CNTD2 antibody, cntd2 antibody
    背景

    Synonyms: CNTD2, CNTD 2, CNTD-2, Cyclin N terminal domain containing 2, Cyclin N terminal domain containing protein 2, FLJ13265, CNTD2_HUMAN.

    Background: CNTD2 (cyclin N-terminal domain containing 2) is a 155 amino acid protein that contains one cyclin N-terminal domain and is encoded by a gene that maps to human chromosome 19q13.2. Chromosome 19 consists of approximately 63 million bases and makes up over 2 % of human genomic DNA. Chromosome 19 is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members, including killer cell and leukocyte Ig-like receptors, various ICAMs, the CEACAM and PSG families, and Fc?receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene Bcl-3.

    基因ID
    79935
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