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MABS275

Sigma-Aldrich

Anti-Gli3 Antibody, clone 5E1

clone 5E1, from mouse

Synonyme(s) :

Transcriptional activator GLI3, GLI3 form of 190 kDa, GLI3-190, GLI3FL, GLI3 C-terminally truncated form, GLI3 form of 83 kDa, GLI3-83

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About This Item

Code UNSPSC :
12352203
eCl@ss :
32160702
Nomenclature NACRES :
NA.41

Source biologique

mouse

Niveau de qualité

Forme d'anticorps

purified immunoglobulin

Type de produit anticorps

primary antibodies

Clone

5E1, monoclonal

Espèces réactives

mouse, human

Technique(s)

immunocytochemistry: suitable
immunohistochemistry: suitable
western blot: suitable

Isotype

IgMκ

Numéro d'accès NCBI

Numéro d'accès UniProt

Conditions d'expédition

wet ice

Modification post-traductionnelle de la cible

unmodified

Informations sur le gène

human ... GLI3(2737)

Catégories apparentées

Description générale

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).

Spécificité

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

Immunogène

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

Application

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.).
Research Category
Signaling
Research Sub Category
Developmental Signaling
This Gli3 antibody is validated for use in WB, ICC & IHC for the detection of the Gli3 protein.

Qualité

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.

Description de la cible

~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.

Forme physique

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

Stockage et stabilité

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

Remarque sur l'analyse

Control
Human thymus tissue lysate

Clause de non-responsabilité

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.

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Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Reet Hunt et al.
Hybridoma (2005), 26(4), 231-240 (2007-08-30)
GLI3 is a transcriptional effector of the developmentally important hedgehog (Hh) signaling pathway. Here we report the production of mouse monoclonal antibody (MAb) against putative repressive motif in GLI3 (GLI3pRM). BALB/c mice were immunized with purified recombinant human GLI3pRM protein
Generation and characterization of a single-chain Fv antibody against G, a hedgehog signaling pathway transcription factor.
Laht, Silja, et al.
Hybridoma (2005), 27, 167-174 (2008)
Jian-Hua Chen et al.
Molecular genetics & genomic medicine, 5(4), 390-404 (2017-07-19)
Alström syndrome (AS), featuring retinal dystrophy, neuronal deafness, cardiomyopathy, metabolic syndrome, and diffuse fibrosis, is caused by biallelic mutations in the centrosomal protein ALMS1. Genotype-phenotype correlation has been suggested without assessment of ALMS1 expression. ALMS1 expression (real-time PCR and immunocytochemistry)

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