Catalog_no | AT6797 |
Product_name | MLXPL rabbit pAb |
Category | 抗原抗体 |
Applications | WB |
Reactivity | Human, Mouse,Rat |
Size | 100μg/50μg/20μg |
Price | 2000.00/1100.00/500.00 |
Gene_name | MLXIPL BHLHD14 MIO WBSCR14 |
Protein_name | MLXPL |
Human swiss prot no | 51085 |
Human swiss prot no | Q9NP71 |
Mouse gene id | 58805 |
Mouse swiss prot no | Q99MZ3 |
Rat gene id | 171078 |
Rat swiss prot no | Q8VIP2 |
immunogen | Synthesized peptide derived from human MLXPL |
Specificity | This antibody detects endogenous levels of MLXPL at Human/Mouse/Rat |
Formulation | Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. |
Source | Rabbit |
Dilution | WB 1:500-2000 |
Purification | The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen. |
Concentration | 1 mg/ml |
Storage_stability | -20°C/1 year |
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], |
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