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EMID1 抗体 (AA 351-441) (FITC)

This anti-EMID1 antibody is a 兔 多克隆 antibody detecting EMID1 in IF (cc) 和 IF (p). Suitable for 大鼠.
产品编号 ABIN6986802
发货至: 中国

Quick Overview for EMID1 抗体 (AA 351-441) (FITC) (ABIN6986802)

抗原

EMID1 (EMI Domain Containing 1 (EMID1))

适用

  • 18
  • 13
  • 4
  • 2
  • 2
  • 2
  • 1
大鼠

宿主

  • 27

克隆类型

  • 27
多克隆

标记

  • 9
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This EMID1 antibody is conjugated to FITC

应用范围

  • 13
  • 12
  • 12
  • 11
  • 3
  • 3
  • 1
Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 8
    • 3
    • 2
    • 1
    • 1
    AA 351-441

    交叉反应

    大鼠

    预测反应

    Human,Mouse,Dog,Cow

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human EMID1

    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

    EMID1 (EMI Domain Containing 1 (EMID1))

    别名

    EMID1

    背景

    Synonyms: AW122071, CO 5, CTA-984G1.2, EMI domain containing 1, EMI domain containing protein 1, EMI domain-containing protein 1, EMI5, EMID 1, Emid1, EMID1_HUMAN, Emilin and multimerin domain containing protein 1, Emilin and multimerin domain-containing protein 1, EMU1, hEmu1, MGC50657, OTTMUSP00000005297, Protein Emu1, Putative emu1, RGD1565846, RP23-338J18.3.

    Background: Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. 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 leukemia.

    基因ID

    129080

    UniProt

    Q96A84
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