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RNF185 抗体 (Cy5)

This anti-RNF185 antibody is a 兔 多克隆 antibody detecting RNF185 in WB 和 IF (p). Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN1419654
发货至: 中国

Quick Overview for RNF185 抗体 (Cy5) (ABIN1419654)

抗原

See all RNF185 抗体
RNF185 (Ring Finger Protein 185 (RNF185))

适用

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  • 25
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  • 2
  • 2
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  • 2
  • 1
  • 1
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人, 小鼠, 大鼠

宿主

  • 35
  • 2

克隆类型

  • 37
多克隆

标记

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  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
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  • 1
  • 1
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This RNF185 antibody is conjugated to Cy5

应用范围

  • 30
  • 12
  • 9
  • 9
  • 3
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 交叉反应

    人, 小鼠, 大鼠

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human RNF185

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 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

    RNF185 (Ring Finger Protein 185 (RNF185))

    别名

    RNF185

    背景

    Synonyms: FLJ38628, Ring finger protein 185, RN185_HUMAN.

    Background: The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in the ubiquitination pathway of protein degradation. RNF185 (ring finger protein 185), also known as FLJ38628, is a 192 amino acid multi-pass membrane protein containing one RING-type zinc finger. Two RNF185 isoforms exist as a result of alternative splicing, and the gene encoding RNF185 maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia.

    基因ID

    91445
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