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WNT1 Polyclonal Antibody

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

货号:E-AB-33231

宿主: Rabbit

反应性: H,M

应用: WB,IHC-p,IF

  • 详情
  • Overview

    Synonyms BMND16,INT1,OI15,oncogene Int1,Proto oncogene protein Wnt 1,Proto-oncogene Int-1 homolog,Proto-oncogene Wnt-1,Wingless type MMTV integration site family member 1,wingless-type MMTV integration site family,member 1 (oncogene INT1),Wnt 1,wnt1,WNT1,Wnt-1抗体
    Swissprot P04628
    Source Rabbit
    Reactivity Human,Mouse
    Immunogen Synthesized peptide derived from the C-terminal region of human Wnt-1
    Application WB(Detection kit: E-IR-R304),IHC-p(Detection kit: E-IR-R213),IF
    Recommended dilution WB,,1:500-1:2000;IHC,,1:100-1:300;IF,,1:200-1:1000;
    Concentration 1mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Secreted>extracellular space>extracellular matrix.
    Isotype IgG
    Purification Affinity purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.02% sodium azide, 0.5% BSA and 50% glycerol, pH7.4
    Background The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is very conserved in evolution, and the protein encoded by this gene is known to be 98% identical to the mouse Wnt1 protein at the amino acid level. The studies in mouse indicate that the Wnt1 protein functions in the induction of the mesencephalon and cerebellum. This gene was originally considered as a candidate gene for Joubert syndrome, an autosomal recessive disorder with cerebellar hypoplasia as a leading feature. However, further studies suggested that the gene mutations might not have a significant role in Joubert syndrome. This gene is clustered with another family member, WNT10B, in the chromosome 12q13 region.
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