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TMEM43 抗体 (AA 195-223)

TMEM43 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB32139 unconjugated
产品编号 ABIN656549
发货至: 中国
  • 抗原 See all TMEM43 抗体
    TMEM43 (Transmembrane Protein 43 (TMEM43))
    抗原表位
    • 6
    • 6
    • 6
    • 6
    • 6
    • 2
    AA 195-223
    适用
    • 21
    • 2
    宿主
    • 21
    克隆类型
    • 21
    多克隆
    标记
    • 7
    • 4
    • 3
    • 3
    • 2
    • 2
    This TMEM43 antibody is un-conjugated
    应用范围
    • 18
    • 16
    • 16
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    预测反应
    M, Rat
    纯化方法
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    免疫原
    This TMEM43 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 195-223 amino acids from the Central region of human TMEM43.
    克隆位点
    RB32139
    亚型
    Ig Fraction
    Top Product
    Discover our top product TMEM43 Primary Antibody
  • 应用备注
    WB: 1:1000. IHC-P: 1:10~50
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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
    TMEM43 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.
    有效期
    6 months
  • 抗原
    TMEM43 (Transmembrane Protein 43 (TMEM43))
    别名
    TMEM43 (TMEM43 产品)
    别名
    zgc:85946 antibody, ARVC5 antibody, ARVD5 antibody, EDMD7 antibody, LUMA antibody, 1200015A22Rik antibody, transmembrane protein 43 antibody, TMEM43 antibody, tmem43 antibody, Tmem43 antibody
    背景
    This gene belongs to the TMEM43 family. Defects in this gene are the cause of familial arrhythmogenic right ventricular dysplasia type 5 (ARVD5), also known as arrhythmogenic right ventricular cardiomyopathy type 5 (ARVC5). Arrhythmogenic right ventricular dysplasia is an inherited disorder, often involving both ventricles, and is characterized by ventricular tachycardia, heart failure, sudden cardiac death, and fibrofatty replacement of cardiomyocytes. This gene contains a response element for PPAR gamma (an adipogenic transcription factor), which may explain the fibrofatty replacement of the myocardium, a characteristic pathological finding in ARVC.
    分子量
    44876
    基因ID
    79188
    NCBI登录号
    NP_077310
    UniProt
    Q9BTV4
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