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RNF215 抗体 (FITC)

RNF215 适用: 人, 小鼠, 大鼠 WB, IF (p) 宿主: 兔 Polyclonal FITC
产品编号 ABIN1401800
发货至: 中国
  • 抗原 See all RNF215 抗体
    RNF215 (Ring Finger Protein 215 (RNF215))
    适用
    人, 小鼠, 大鼠
    宿主
    • 28
    • 1
    克隆类型
    • 29
    多克隆
    标记
    • 6
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This RNF215 antibody is conjugated to FITC
    应用范围
    • 29
    • 12
    • 12
    • 12
    • 5
    • 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 RNF215
    亚型
    IgG
    Top Product
    Discover our top product RNF215 Primary Antibody
  • 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
    RNF215 (Ring Finger Protein 215 (RNF215))
    别名
    RNF215 (RNF215 产品)
    别名
    RGD1310738 antibody, 0610009J22Rik antibody, AW557025 antibody, C77903 antibody, ring finger protein 215 antibody, Rnf215 antibody, RNF215 antibody
    背景

    Synonyms: RING finger protein 215, Rnf215, RN215_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. RNF215 (ring finger protein 215), is a 377 amino acid multi-pass membrane protein containing one RING-type zinc finger. The gene encoding RNF215 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
    200312
    UniProt
    Q9Y6U7
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