GLI3 Antibody (monoclonal) (M01)
Mouse monoclonal antibody raised against a partial recombinant GLI3.
|Application ||WB, IF, E|
|Calculated MW||169863 Da|
|Other Names||Transcriptional activator GLI3, GLI3 form of 190 kDa, GLI3-190, GLI3 full length protein, GLI3FL, Transcriptional repressor GLI3R, GLI3 C-terminally truncated form, GLI3 form of 83 kDa, GLI3-83, GLI3|
|Target/Specificity||GLI3 (NP_000159, 1 a.a. ~ 110 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.|
|Format||Clear, colorless solution in phosphate buffered saline, pH 7.2 .|
|Storage||Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.|
|Precautions||GLI3 Antibody (monoclonal) (M01) is for research use only and not for use in diagnostic or therapeutic procedures.|
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This gene encodes a protein which belongs to the C2H2-type zinc finger proteins subclass of the Gli family. They are characterized as DNA-binding transcription factors and are mediators of Sonic hedgehog (Shh) signaling. The protein encoded by this gene localizes in the cytoplasm and activates patched Drosophila homolog (PTCH) gene expression. It is also thought to play a role during embryogenesis. Mutations in this gene have been associated with several diseases, including Greig cephalopolysyndactyly syndrome, Pallister-Hall syndrome, preaxial polydactyly type IV, and postaxial polydactyly types A1 and B.
Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations. Johnston JJ, et al. Hum Mutat, 2010 Jul 29. PMID 20672375.Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia. Jugessur A, et al. PLoS One, 2010 Jul 9. PMID 20634891.Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility. Lascorz J, et al. Carcinogenesis, 2010 Sep. PMID 20610541.Human intronic enhancers control distinct sub-domains of Gli3 expression during mouse CNS and limb development. Abbasi AA, et al. BMC Dev Biol, 2010 Apr 28. PMID 20426846.Birth defects caused by mutations in human GLI3 and mouse Gli3 genes. Naruse I, et al. Congenit Anom (Kyoto), 2010 Mar. PMID 20201963.
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