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GRAMD2 抗体 (AA 151-250) (AbBy Fluor® 555)

This AbBy Fluor® 555-conjugated 兔 多克隆 anti-GRAMD2 antibody specifically detects GRAMD2 in WB, IF (cc) 和 IF (p). The antibody is reactive with 大鼠 samples.
产品编号 ABIN1399835
发货至: 中国
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Quick Overview for GRAMD2 抗体 (AA 151-250) (AbBy Fluor® 555) (ABIN1399835)

抗原

GRAMD2 (GRAM Domain Containing 2 (GRAMD2))

适用

  • 15
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
大鼠

宿主

  • 18

克隆类型

  • 18
多克隆

标记

  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GRAMD2 antibody is conjugated to AbBy Fluor® 555

应用范围

  • 18
  • 12
  • 12
  • 4
  • 3
  • 3
  • 1
Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 2
    • 1
    AA 151-250

    交叉反应

    大鼠

    预测反应

    Human,Mouse,Dog,Cow,Sheep,Horse,Chicken

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human GRAMD2

    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

    GRAMD2 (GRAM Domain Containing 2 (GRAMD2))

    别名

    GRAMD2

    背景

    Synonyms: GRAM domain containing 2, GRAM domain containing protein 2, GRAMD 2, GRAM2_HUMAN.

    Background: GRAMD2 is a 354 amino acid single-pass membrane protein that contains one GRAM domain and is encoded by a gene that maps to human chromosome 15q23. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.

    基因ID

    196996
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