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IGF1 Polyclonal Antibody

规格: / 60μL / 120μL / 200μL
价格: / ¥1380 / ¥2220 / ¥3300

货号:E-AB-70301

宿主: Rabbit

反应性: H

应用: IHC

  • 详情
  • Overview

    Synonyms IBP1,IGF I,IGF IA,IGF IB,IGF-I,Igf1,IGF1,IGF1A,IGFI,IGFIA,Insulin like growth factor 1 (somatomedin C),Insulin like growth factor 1,Insulin like growth factor IA,Insulin like growth factor IB,Insulin-like growth factor I,Mechano growth factor,MGF,OTTHUMP00000195080,OTTHUMP00000195081,OTTHUMP00000195082,OTTHUMP00000195083,OTTHUMP00000195084,Somatomedia C,Somatomedin C,Somatomedin-C,IGF1抗体
    Swissprot P05017
    Source Rabbit
    Reactivity Human
    Immunogen KLH conjugated Synthetic peptide corresponding to Mouse IGF1
    Application IHC(Detection kit: E-IR-R213)
    Recommended dilution IHC,,1:300-1:1000
    Concentration 1 mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Secreted
    Tissue specificity Highest expression level in stria vascularis of cochlear duct
    Isotype IgG
    Purification Affinity purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.02% sodium azide,100 μg/ml BSA and 50% glycerol.
    Background IGF1, also named as IBP1, MGF, IGF-IA and Somatomedin-C, belongs to the insulin family. IGF1 is structurally and functionally related to insulin but have a much higher growth-promoting activity. Altered expression or mutation of IGF-1 is associated with several human disorders, including type I diabetes and various forms of cancer. Defects in IGF1 are the cause of insulin-like growth factor I deficiency (IGF1 deficiency) which is an autosomal recessive disorder characterized by growth retardation, sensorineural deafness and mental retardation. The antibody is specific to isoform IGF-1A.
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