ELK Biotechnology
MLXPL Rabbit Polyclonal Antibody - ES14932
MLXPL Rabbit Polyclonal Antibody - ES14932
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MLXPL Rabbit Polyclonal Antibody
Sizes: 50μL, 100μL
Catalogue Numbers: ES14932-50, ES14932-100
Lead times: 1-2 weeks, if manufacturer has product in stock
Manufacturer/Ship Location: China
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],
Reactivity: Human, Mouse, Rat
Host: Rabbit
Applications: WB, ELISA, IHC
Clonality: Polyclonal
Immunogen: Synthesized peptide derived from human MLXPL AA range: 303-353
Isotype: IgG
Target: MLXPL
Specificity: This antibody detects endogenous levels of MLXPL at Human/Mouse/Rat
Dilution: WB 1:500-2000, IHC-p 1:50-300, ELISA 2000-20000
Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Concentration: 1 mg/ml,
Formlation: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Expression: Expressed in liver, heart, kidney, cerebellum and intestinal tissues,
Molecular Weight (Da): 94kD
Fields: Insulin resistance, Non-alcoholic fatty liver disease
Function: Disease: 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
Subcellular Location: Nucleus
Storage and Stability: -20°C/1 year
Gene Name: MLXIPL BHLHD14 MIO WBSCR14
Protein Name: MLXPL
Mouse Gene ID: 58805
Mouse SwissProt Number: Q99MZ3
Rat Gene ID: 171078
Rat SwissProt Number: Q8VIP2
Research Use Only
