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

RBM28 抗体 (AA 18-584)

The 兔 多克隆 anti-RBM28 antibody is suitable to detect RBM28 in samples from 人. It has been validated for WB, ELISA 和 FACS.
产品编号 ABIN7871430
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 RBM28 抗体 (AA 18-584) (ABIN7871430)

抗原

See all RBM28 抗体
RBM28 (RNA Binding Motif Protein 28 (RBM28))

适用

  • 24
  • 5
  • 5
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1

宿主

  • 24

克隆类型

  • 24
多克隆

标记

  • 19
  • 1
  • 1
  • 1
  • 1
  • 1
This RBM28 antibody is un-conjugated

应用范围

  • 24
  • 11
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • 抗原表位

    • 8
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 18-584

    原理

    RBM28 Antibody / RNA-binding protein 28

    纯化方法

    Antigen affinity purified

    免疫原

    Recombinant human protein (amino acids E18-K584) was used as the immunogen for the RBM28 antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the RBM28 antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Lyophilized

    缓冲液

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    储存条件

    4 °C,-20 °C

    储存方法

    After reconstitution, the RBM28 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • 抗原

    RBM28 (RNA Binding Motif Protein 28 (RBM28))

    别名

    RBM28

    背景

    RNA-binding protein 28 is a protein that in humans is encoded by the RBM28 gene. The protein encoded by this gene is a specific nucleolar component of the spliceosomal small nuclear ribonucleoprotein (snRNP)complexes . It specifically associates with U1, U2, U4, U5, and U6 small nuclear RNAs (snRNAs), possibly coordinating their transition through the nucleolus. Mutation in this gene causes alopecia, progressive neurological defects, and endocrinopathy (ANE syndrome), a pleiotropic and clinically heterogeneous disorder. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

    UniProt

    Q9NW13

    途径

    SARS-CoV-2 Protein Interactome
You are here: