Anti-Gli3; clone 5E1

Code: MABS275 D2-231

Analysis Note

ControlHuman thymus tissue lysate

Application

This Gli3 antibody is validated for use in WB, ICC & IHC for the detection of the Gli...


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Analysis Note

ControlHuman thymus tissue lysate

Application

This Gli3 antibody is validated for use in WB, ICC & IHC for the detection of the Gli3 protein.

Research CategorySignaling

Research Sub CategoryDevelopmental Signaling

Immunocytochemistry Analysis: A representative lot detected Gli3 in PK-15, COS-1, and TM4 cells cotransfected with recombinant Gli3 (Hunt, R., et al. (2007). Hybridoma. 27(4):231-240.).

Immunohistochemistry Analysis: A representative lot detected Gli3 in mouse embryo cross-sections (Laht, S., et al. (2008). Hybridoma. 27(3):167-174.).

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

General description

Gli3 can function as both a transcriptional activator and repressor of the sonic hedgehog (Shh) pathway. The full-length Gli3 form (GLI3FL) becomes an activator (GLI3A) after phosphorylation and nuclear translocation. The C-terminally truncated form (GLI3R), acts as a repressor. Proper balance between the Gli3 activator and the repressor specifies limb digit number and identity during development. In concert with TRPS1, Gli3 plays a role in activating chondrocyte proliferation. Gli3 is expressed in several normal adult tissues, including lung, colon, spleen, placenta, testis, and myometrium. Gli3 defects are associated with Greig cephalo-poly-syndactyly syndrome (GCPS), Pallister-Hall syndrome (PHS), polydactyly postaxial type A1 (PAPA1), polydactyly postaxial type B polydactyly (PAPB), and polydactyly preaxial type 4 (POP4).

Immunogen

Recombinant protein corresponding to the putative repressive motif of human GLI3.

Physical form

Purified by Ion-Exchange Chromatography

Purified mouse monoclonal IgMκ in buffer containing PBS with 0.05% sodium azide.

Format: Purified

Quality

Evaluated by Western Blotting in human thymus tissue lysate.

Western Blotting Analysis: A 1:1,000 dilution from a representative lot detected in Gli3 in 10 µg of human thymus tissue lysate.

Specificity

This antibody recognizes the truncated, repressor form and the full length protein of human Gli3.

Storage and Stability

Stable for 1 year at 2-8°C from date of receipt.

Target description

~75 kDa and ~200 kDa observed. The truncated, repressor form and full length form of this protein has been observed at ~83 kDa and ~190 kDa, respectively (Tanimoto, Y., et al. (2012). J Biol Chem. 287(25):21429-21438.). Uncharacterized bands may be observed at ~160 kDa and below ~50 kDa in some cell lysates.

antibody formpurified immunoglobulin
antibody product typeprimary antibodies
biological sourcemouse
clone5E1, monoclonal
Gene Informationhuman ... GLI3(2737)
isotypeIgMκ
NCBI accession no.NP_000159.3
Quality Level100
shipped inwet ice
species reactivityhuman, mouse
technique(s)immunocytochemistry: suitable, western blot: suitable, immunohistochemistry: suitable
UniProt accession no.P10071
This product has met the following criteria to qualify for the following awards:



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