SKU: WR6046 Categories: ,

U-Blot® TGIF Rabbit mAb

Price range: $268.00 through $328.00

SKU: WR6046-50
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Product details

Background:
The protein encoded by this gene is a member of the three-amino acid loop extension (TALE) superclass of atypical homeodomains. TALE homeobox proteins are highly conserved transcription regulators. This particular homeodomain binds to a previously characterized retinoid X receptor responsive element from the cellular retinol-binding protein II promoter. In addition to its role in inhibiting 9-cis-retinoic acid-dependent RXR alpha transcription activation of the retinoic acid responsive element , the protein is an active transcriptional co-repressor of SMAD2 and may participate in the transmission of nuclear signals during development and in the adult. Mutations in this gene are associated with holoprosencephaly type 4 , which is a structural anomaly of the brain. Alternative splicing has been observed at this locus and multiple splice variants encoding distinct isoforms are described. [provide

Specifications

Size50μL/100μL
TargetTGIF
ReactivityHuman, Mouse
ApplicationsWB, IF, IP, ELISA
MW(Calculated)43kD
MW(Observed)32-34kD
Host SpeciesRabbit
IsotypeIgG, Kappa
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:2000-1:10000; IF 1:200-1:1000; ELISA 1:5000-1:20000; IP 1:50-1:200
FormulationPBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
PurificationRecombinant Antibody expressed in animal component-free (ACF) media, purified via Protein A affinity chromatography.
Storage-15°C to -25°C/1 year (Do not lower than -25°C)
Concentration
ClonalityMonoclonal
Clone NumberRM2033R
ImmunogenThe specific immunogen used to produce this antibody is proprietary information.
SpecificityEndogenous
Gene NameTGIF1
Protein NameHomeobox protein TGIF1
Other NameTGIF1; / TGIF; / Homeobox protein TGIF1; / 5'-TG-3'-interacting factor 1
SpeciesHuman
Gene ID7050
UniprotQ15583,
Species.1Mouse
Gene ID.121815
Uniprot.1P70284
Species.2
Gene ID.2
Uniprot.2
Cellular LocalizationNucleus.
Tissue ExpressionBrain ,Liver ,Placenta ,
Signaling_pathwayEnvironmental Information Processing >> Signal transduction >> TGF-beta signaling pathway
Research Areas>>TGF-beta signaling pathway
FunctionDisease:Defects in TGIF1 are the cause of holoprosencephaly type 4 (HPE4) [MIM:142946]. Holoprosencephaly (HPE) [MIM:236100] is the most common structural anomaly of the brain , in which the developing forebrain fails to correctly separate into right and left hemispheres. Holoprosencephaly is genetically heterogeneous and associated with several distinct facies and phenotypic variability. ,Function:Binds to a retinoid X receptor (RXR) responsive element from the cellular retinol-binding protein II promoter (CRBPII-RXRE) . Inhibits the 9-cis-retinoic acid-dependent RXR alpha transcription activation of the retinoic acid responsive element. Active transcriptional corepressor of SMAD2. Links the nodal signaling pathway to the bifurcation of the forebrain and the establishment of ventral midline structures. May participate in the transmission of nuclear signals during development and in the adult , as illustrated by the down-modulation of the RXR alpha activities. ,similarity:Belongs to the TALE/TGIF homeobox family. ,similarity:Contains 1 homeobox DNA-binding domain. ,subunit:Interacts with CTBP , SMAD2 , SMAD3 and HDAC1. ,
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