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DMPK 抗体 (N-Term) (FITC)

This 兔 多克隆 antibody specifically detects DMPK in FACS. It exhibits reactivity toward 小鼠 和 大鼠.
产品编号 ABIN7986717
发货至: 中国
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Quick Overview for DMPK 抗体 (N-Term) (FITC) (ABIN7986717)

抗原

See all DMPK 抗体
DMPK (Dystrophia Myotonica-Protein Kinase (DMPK))

适用

  • 42
  • 34
  • 17
  • 2
  • 2
  • 2
  • 1
  • 1
小鼠, 大鼠

宿主

  • 64
  • 8

克隆类型

  • 66
  • 6
多克隆

标记

  • 30
  • 5
  • 5
  • 4
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This DMPK antibody is conjugated to FITC

应用范围

  • 38
  • 24
  • 13
  • 13
  • 10
  • 10
  • 6
  • 6
  • 5
  • 5
  • 3
  • 1
Flow Cytometry (FACS)
  • 抗原表位

    • 16
    • 15
    • 8
    • 5
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    N-Term

    原理

    Anti-DMPK Antibody FITC Conjugated

    交叉反应 (详细)

    No cross-reactivity with other proteins

    纯化方法

    Immunogen affinity purified.

    免疫原

    A synthetic peptide corresponding to a sequence at the N-terminus of human DMPK.

    亚型

    IgG
  • 应用备注

    Flow Cytometry, Optimal dilutions should be determined by end users.

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

    有效期

    12 months
  • 抗原

    DMPK (Dystrophia Myotonica-Protein Kinase (DMPK))

    别名

    DMPK

    背景

    Background: The protein encoded by this gene is a serine/threonine protein kinase that contains coiled-coil and C-terminal membrane association domains. In the embryonic mouse, it is found in cardiac and skeletal myocytes where it appears to play a role in myogenesis. In adults, the transcript is localized to several tissues including brain, heart, and skeletal and smooth muscle, and a function in cytoskeletal remodeling has been described. Transcripts with expanded CUG repeats in the 3' untranslated region mediate alternative splicing of several genes and sequester RNA binding proteins and RNA transcripts that contain CAG repeats, resulting in myotonic dystrophy, an autosomal dominant neuromuscular disorder. Alternative splicing results in multiple protein coding and non-coding transcript variants.

    Gene Full Name: dystrophia myotonica-protein kinase

    基因ID

    13400

    UniProt

    P54265

    途径

    Regulation of Muscle Cell Differentiation, Synaptic Membrane, Skeletal Muscle Fiber Development
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