IGF-I rabbit pAb
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IGF-I rabbit pAb
Background:
The protein encoded by this gene is similar to insulin in function and structure and is a member of a family of proteins involved in mediating growth and development. The encoded protein is processed from a precursor, bound by a specific receptor, and secreted. Defects in this gene are a cause of insulin-like growth factor I deficiency. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar processing to generate mature protein. [provided by RefSeq, Sep 2015]Description:
The protein encoded by this gene is similar to insulin in function and structure and is a member of a family of proteins involved in mediating growth and development. The encoded protein is processed from a precursor, bound by a specific receptor, and secreted. Defects in this gene are a cause of insulin-like growth factor I deficiency. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar processing to generate mature protein. [provided by RefSeq, Sep 2015],UniProt:
P01343/P05019Swiss Prot:
P01343/P05019Reactivity:
Human; Mouse; RatImmunogen:
The antiserum was produced against synthesized peptide derived from human IGF-I. AA range:100-149Clonality:
PolyclonalSource:
RabbitApplications:
IHC; IF; ELISAConcentration:
1 mg/mlDilution:
Immunohistochemistry: 1/100 - 1/300. ELISA: 1/10000. Not yet tested in other applications.Storage Conditions:
-20°C/1 yearFragment:
IgGSubcellular Location:
Extracellular region, extracellular space, plasma membrane, insulin-like growth factor binding protein complex, platelet alpha granule lumen, alphav-beta3 integrin-IGF-1-IGF1R complex, insulin-like growth factor ternary complex, exocytic vesicleOther Product Names:
IBP1; IGF-IA; IGF1A; IGFI; insulin-like growth factor 1; insulin-like growth factor IA; mechano growth factor; MGF; somatomedin CGene ID (Human):
3479
