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FUNDC2 抗体

FUNDC2 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7246850
发货至: 中国
  • 抗原 See all FUNDC2 抗体
    FUNDC2 (FUN14 Domain Containing 2 (FUNDC2))
    适用
    • 15
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    宿主
    • 14
    • 3
    克隆类型
    • 15
    • 2
    多克隆
    标记
    • 10
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FUNDC2 antibody is un-conjugated
    应用范围
    • 10
    • 4
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Antigen affinity purification
    免疫原
    Fusion protein of human FUNDC2
    亚型
    IgG
    Top Product
    Discover our top product FUNDC2 Primary Antibody
  • 应用备注
    IHC 1:50-1:300, ELISA 1:5000-1:10000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.72 mg/mL
    缓冲液
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    FUNDC2 (FUN14 Domain Containing 2 (FUNDC2))
    别名
    FUNDC2 (FUNDC2 产品)
    别名
    DC44 antibody, HCBP6 antibody, HCC3 antibody, PD03104 antibody, 4833415N24Rik antibody, FUN14 domain containing 2 antibody, FUNDC2 antibody, Fundc2 antibody
    背景
    FUNDC2 (FUN14 domain-containing protein 2), also known as HCC-3 (cervical cancer proto-oncogene 3 protein), HCBP6 (hepatitis C virus core-binding protein 6) or DC44, is a 189 amino acid protein belonging to the FUN14 family. The gene encoding FUNDC2 maps to human chromosome Xq28. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
    UniProt
    Q9BWH2
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