MLXIPL Antikörper (AA 17-175)
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- Target Alle MLXIPL Antikörper anzeigen
- MLXIPL (MLX Interacting Protein-Like (MLXIPL))
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Bindungsspezifität
- AA 17-175
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser MLXIPL Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB)
- Sequenz
- VAPSPDSDSD TDSEDPSLRR SAGGLLRSQV IHSGHFMVSS PHSDSLPRRR DQEGSVGPSD FGPRSIDPTL TRLFECLSLA YSGKLVSPKW KNFKGLKLLC RDKIRLNNAI WRAWYIQYVK RRKSPVCGFV TPLQGPEADA HRKPEAVVLE GNYWKRRIE
- Kreuzreaktivität
- Human, Maus
- Produktmerkmale
- Polyclonal Antibodies
- Immunogen
- Recombinant fusion protein containing a sequence corresponding to amino acids 17-175 of human MLXIPL (NP_116569.1).
- Isotyp
- IgG
- Top Product
- Discover our top product MLXIPL Primärantikörper
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- Applikationshinweise
- WB,1:500 - 1:2000
- Kommentare
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HIGH QUALITY
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Buffer
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- MLXIPL (MLX Interacting Protein-Like (MLXIPL))
- Andere Bezeichnung
- MLXIPL (MLXIPL Produkte)
- Synonyme
- ChREBP antikoerper, MLXIPL antikoerper, CHREBP antikoerper, MIO antikoerper, MONDOB antikoerper, WBSCR14 antikoerper, WS-bHLH antikoerper, bHLHd14 antikoerper, Wbscr14 antikoerper, MLX interacting protein-like antikoerper, MLX interacting protein like antikoerper, MLXIPL antikoerper, Mlxipl antikoerper
- Hintergrund
- 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.,MLXIPL,CHREBP,MIO,MLX,MONDOB,WBSCR14,WS-bHLH,bHLHd14,Epigenetics & Nuclear Signaling,Transcription Factors,Cancer,Endocrine & Metabolism,Endocrine and metabolic diseases,Diabetes,Cardiovascular,Heart,Cardiovascular diseases,Heart disease,MLXIPL
- Molekulargewicht
- 62 kDa/78 kDa/90 kDa/92 kDa/93 kDa
- Gen-ID
- 51085
- UniProt
- Q9NP71
- Pathways
- Carbohydrate Homeostasis, Regulation of Carbohydrate Metabolic Process
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