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  2. Polyclonal

GTX64439

ChREBP antibody

Cannot supply to this region.

SKU:
GTX64439
Additional Names:
MLX interacting protein like , CHREBP , MIO , MLX , MONDOB , WBSCR14 , WS-bHLH , bHLHd14
Application:
WB
Physical State:
Liquid
Species Reactivity:
Human
Purification:
Affinity Purified
Storage Conditions:
-20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Supplier:
Genetex
Host:
Rabbit
Reactivities:
Human, Mouse
Buffer:
PBS, 50% Glycerol, 0.02% Sodium azide.
Immunogen:
Recombinant fusion protein containing a sequence corresponding to amino acids 17-175 of human MLXIPL (NP_116569.1).
Uniprot:
Q9NP71
Synonyms:
bHLHd14;carbohydrate response element binding protein;carbohydrate-responsive element-binding protein;CHREBP;class D basic helix-loop-helix protein 14;MIO;MLX;Mlx interactor;MLX-interacting protein-like;MONDOB;WBSCR14;Williams Beuren syndrome chromosome region 14;williams-Beuren syndrome chromosomal region 14 protein;Williams-Beuren syndrome chromosome region 14 protein 1;Williams-Beuren syndrome chromosome region 14 protein 2;Williams-Beuren syndrome chromosome region 14 protein 3;WS basic-helix-loop-helix leucine zipper protein;WS-bHLH
Extra Details:
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]
Shipping Conditions:
Blue Ice