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IHH Antibody (N-term) Blocking Peptide

Synthetic peptide

     
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Product Information
Primary Accession Q14623
Clone Names 100525049
Additional Information
Gene ID 3549
Other Names Indian hedgehog protein, IHH, HHG-2, Indian hedgehog protein N-product, Indian hedgehog protein C-product, IHH
Format Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
StorageMaintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.
PrecautionsThis product is for research use only. Not for use in diagnostic or therapeutic procedures.
Protein Information
Name IHH (HGNC:5956)
Function [Indian hedgehog protein]: The C-terminal part of the indian hedgehog protein precursor displays an autoproteolysis and a cholesterol transferase activity (By similarity). Both activities result in the cleavage of the full-length protein into two parts followed by the covalent attachment of a cholesterol moiety to the C- terminal of the newly generated N-product (By similarity). Both activities occur in the reticulum endoplasmic (By similarity). Plays a role in hedgehog paracrine signaling (PubMed:24342078). Associated with the very-low-density lipoprotein (VLDL) particles to function as a circulating morphogen for endothelial cell integrity maintenance (PubMed:20839884).
Cellular Location [Indian hedgehog protein N-product]: Cell membrane; Lipid-anchor {ECO:0000250|UniProtKB:Q62226}. Note=The N-product remains associated with the cell surface. {ECO:0000250|UniProtKB:Q15465}
Tissue Location Expressed in embryonic lung, and in adult kidney and liver
Research Areas
Citations (0)
citation

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Background

This gene encodes a member of the hedgehog family ofsecreted signaling molecules. Hedgehog proteins are essentialregulators of a variety of developmental processes includinggrowth, patterning and morphogenesis. The encoded proteinspecifically plays a role in bone growth an differentiation.Mutations in this gene are the cause of brachydactyly type A1 whichis characterized by shortening or malformation of the phalanges.Mutations in this gene are also the cause of acrocapitofemoraldysplasia.

References

Meulenbelt, I., et al. Ann. Rheum. Dis. (2010) In press :Kang, S.J., et al. Hum. Mol. Genet. 19(13):2725-2738(2010)Okada, Y., et al. Hum. Mol. Genet. 19(11):2303-2312(2010)Zhao, J., et al. BMC Med. Genet. 11, 96 (2010) :Chuang, P.T., et al. Nature 397(6720):617-621(1999)

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$ 277.78
Cat# BP14935a
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