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PNKD 抗体 (AA 140-220)

This 兔 多克隆 antibody specifically detects PNKD in ELISA 和 WB. It exhibits reactivity toward 人 和 小鼠.
产品编号 ABIN7230718
发货至: 中国
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Quick Overview for PNKD 抗体 (AA 140-220) (ABIN7230718)

抗原

See all PNKD 抗体
PNKD (Paroxysmal Nonkinesigenic Dyskinesia (PNKD))

适用

  • 19
  • 18
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
人, 小鼠

宿主

  • 25
  • 1

克隆类型

  • 25
多克隆

标记

  • 17
  • 3
  • 2
  • 2
  • 1
  • 1
This PNKD antibody is un-conjugated

应用范围

  • 19
  • 17
  • 12
  • 3
  • 1
  • 1
ELISA, Western Blotting (WB)
  • 抗原表位

    • 8
    • 6
    • 6
    • 2
    • 1
    • 1
    • 1
    AA 140-220

    原理

    PNKD Polyclonal Antibody

    特异性

    The antibody detects endogenous levels of PNKD protein

    纯化方法

    The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

    免疫原

    Synthesized peptide derived from part region of human PNKD protein at AA range: 140-220

    亚型

    IgG
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

    说明

    Primary Antibody

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

    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

    Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
  • 抗原

    PNKD (Paroxysmal Nonkinesigenic Dyskinesia (PNKD))

    别名

    PNKD

    背景

    Rabbit Anti-PNKD Polyclonal Antibody,Probable hydrolase PNKD, Myofibrillogenesis regulator 1, MR-1, Paroxysmal nonkinesiogenic dyskinesia protein, Trans-activated by hepatitis C virus core protein 2,PNKD (Paroxysmal Nonkinesigenic Dyskinesia) is a Protein Coding gene. Diseases associated with PNKD include Familial Paroxysmal Nonkinesigenic Dyskinesia and Paroxysmal Nonkinesigenic Dyskinesia 1. PNKD is thought to play a role in the regulation of myofibrillogenesis. Mutations in PNKD have been associated with the movement disorder paroxysmal non-kinesigenic dyskinesia. Alternative splicing results in multiple transcript variants.,PNKD

    分子量

    observerd band 42kDa

    基因ID

    25953

    UniProt

    Q8N490
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