电话:
+86 (0512) 65829739
传真:
+86 (010) 6788 5057
电子邮件:
orders@antibodies-online.cn

Rubicon 抗体 (AA 859-972)

This anti-Rubicon antibody is a 小鼠 单克隆 antibody detecting Rubicon in ELISA. Suitable for 人.
产品编号 ABIN7193445
发货至: 中国
Contact our Customer Service for availability and price in your country. Contact Info

Our Local Distributor

中国
北京 101111
No. 88 KeChuang 6th Street
Beijing Economic Technological Development Area
Room 801-803
4A Biotech Co.,Ltd.
Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for Rubicon 抗体 (AA 859-972) (ABIN7193445)

抗原

See all Rubicon (KIAA0226) 抗体
Rubicon (KIAA0226) (KIAA0226)

适用

  • 30
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1

宿主

  • 29
  • 1
小鼠

克隆类型

  • 29
  • 1
单克隆

标记

  • 18
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Rubicon antibody is un-conjugated

应用范围

  • 25
  • 15
  • 14
  • 10
  • 9
  • 5
  • 5
  • 3
ELISA

克隆位点

4F5B5
  • 抗原表位

    • 13
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 859-972

    原理

    RUBCN Antibody

    纯化方法

    Purified antibody

    免疫原

    Purified recombinant fragment of human RUBCN (AA: 859-972) expressed in E. Coli.

    亚型

    IgG1
  • 应用备注

    ELISA: 1/10000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Purified antibody in PBS with 0.05 % 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

    4 °C,-20 °C

    储存方法

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • 抗原

    Rubicon (KIAA0226) (KIAA0226)

    别名

    RUBCN

    背景

    The protein encoded by this gene is a negative regulator of autophagy and endocytic trafficking and controls endosome maturation. This protein contains two conserved domains, an N-terminal RUN domain and a C-terminal DUF4206 domain. The RUN domain is involved in Ras-like GTPase signaling, and the DUF4206 domain contains a diacylglycerol (DAG) binding-like motif. Mutation in this gene results in deletion of the DAG binding-like motif and causes a recessive ataxia. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.

    分子量

    108.6 kDa

    基因ID

    9711

    UniProt

    Q92622

    途径

    Autophagy
You are here: