SKU: WP16663 Categories: ,

MLXPL rabbit pAb

Price range: $268.00 through $328.00

SKU: WP16663-100
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Product details

Background:

This gene encodes a basic helix-loop-helix leucine zipper transcription factor of the Myc/Max/Mad superfamily. This protein forms a heterodimeric complex and binds and activates, in a glucose-dependent manner, carbohydrate response element (ChoRE) motifs in the promoters of triglyceride synthesis genes. The gene is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015],

Specifications

Size50μL/100μL
TargetMLXPL
ReactivityHuman, Mouse, Rat
ApplicationsWB, ELISA, IHC
MW(Calculated)94kD
MW(Observed)
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-2000; IHC 1:50-300; ELISA 1:2000-20000 / Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#WT1004)
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenSynthesized peptide derived from human MLXPL AA range: 303-353
SpecificityThis antibody detects endogenous levels of MLXPL at Human/Mouse/Rat
Gene NameMLXIPL BHLHD14 MIO WBSCR14
Protein NameMLXPL
Other Name
SpeciesHuman
Gene ID51085
UniprotQ9NP71,
Species.1Mouse
Gene ID.158805
Uniprot.1Q99MZ3,
Species.2Rat
Gene ID.2171078
Uniprot.2Q8VIP2
Cellular LocalizationNucleus.
Tissue ExpressionExpressed in liver, heart, kidney, cerebellum and intestinal tissues.
Signaling_pathway
Research Areas>>Insulin resistance; / >>Non-alcoholic fatty liver disease
FunctionDisease:Haploinsufficiency of WBSCR14 may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in Williams-Beuren syndrome (WBS) [MIM:194050]. WBS is a rare developmental disorder. It is a contiguous gene deletion syndrome involving genes from chromosome band 7q11.23.,Function:Transcriptional repressor. Binds to the canonical and non-canonical E box sequences 5'-CACGTG-3'.,similarity:Contains 1 basic helix-loop-helix (bHLH) domain.,subunit:Binds DNA as a heterodimer with TCFL4/MLX.,tissue specificity:Expressed in liver, heart, kidney, cerebellum and intestinal tissues.,
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