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FUNDC2 Polyclonal Antibody

规格: / 20μL / 60μL / 120μL / 200μL
价格: / ¥420 / ¥1010 / ¥1640 / ¥2365

货号:E-AB-18928

宿主: Rabbit

反应性: H

应用: IHC

  • 详情
  • Overview

    Synonyms Cervical cancer oncogene 3,Cervical cancer proto oncogene 3 protein,DC44,FLJ33773,FUN14 domain containing 2,FUN14 domain containing protein 2,FUNDC 2,HCBP 6,HCBP6,HCC 3,HCC3,Hepatitis C virus core binding protein 6,MGC131676,MGC2495,OTTHUMP00000015441,OTTHUMP00000061459,PD03104,FUNDC2抗体
    Swissprot Q9BWH2
    Source Rabbit
    Reactivity Human
    Immunogen Fusion protein of human FUNDC2
    Application IHC(Detection kit: E-IR-R213)
    Recommended dilution IHC,,1:50-1:300
    Concentration 0.72mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Mitochondrial
    Isotype IgG
    Purification Affinity purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.05% NaN3 and 40% Glycerol,pH7.4
    Background 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.
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