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Dymeclin 抗体 (AA 151-250) (Cy5.5)

This anti-Dymeclin antibody is a 兔 多克隆 antibody detecting Dymeclin in WB, IF (cc) 和 IF (p). Suitable for 人 和 大鼠.
产品编号 ABIN1706603
发货至: 中国

Quick Overview for Dymeclin 抗体 (AA 151-250) (Cy5.5) (ABIN1706603)

抗原

See all Dymeclin (DYM) 抗体
Dymeclin (DYM)

适用

  • 35
  • 15
  • 3
人, 大鼠

宿主

  • 29
  • 6
  • 1
  • 1

克隆类型

  • 30
  • 7
多克隆

标记

  • 17
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Dymeclin antibody is conjugated to Cy5.5

应用范围

  • 32
  • 13
  • 12
  • 12
  • 12
  • 9
  • 8
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 5
    • 5
    • 1
    • 1
    • 1
    • 1
    AA 151-250

    交叉反应

    人, 大鼠

    预测反应

    Mouse,Dog,Cow,Sheep,Horse

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human Dymeclin

    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

    Dymeclin (DYM)

    别名

    Dymeclin

    背景

    Synonyms: DMC, Dyggve-Melchior-Clausen syndrome protein, DYM, FLJ20071, FLJ90130, SMC, DYM_HUMAN.

    Background: Dyggve-Melchior-Clausen syndrome (DMC), a rare autosomal recessive disorder, is characterized by microcephaly, short trunk dwarfism and sometime psychomotor retardation. Cutaneous cells of affected individuals show dilated rough endoplasmic reticulum and enlarged vacuoles. The Dyggve-Melchior-Clausen syndrome protein, also designated dymeclin, may play a role in proteoglycan metabolism and intracellular protein digestion. It is a widely expressed multi-pass membrane protein, detected primarily in chondrocytes and fetal brain tissue. Defects in dymeclin are also the cause of Smith-McCort dysplasis syndrome (SMC), which has characteristics identical to those of Dyggve-Melchior-Clausen syndrome.

    基因ID

    54808
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