MLXIPL antibody (C-Term)

Catalog No. ABIN656493

The Rabbit Polyclonal anti-MLXIPL antibody (Clone RB31107) (ABIN656493) specifically detects MLXIPL in WB and IHC (p). The antibody is reactive with Human and Mouse samples.

Quick Overview for MLXIPL antibody (C-Term) (ABIN656493)

Target: MLXIPL (MLX Interacting Protein-Like (MLXIPL))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MLXIPL antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone: RB31107

Product Details anti-MLXIPL Antibody

Binding Specificity: AA 624-653, C-Term

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This MLXIPL antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 624-653 amino acids from the C-terminal region of human MLXIPL.

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:2000. WB: 1:2000. IHC-P: 1:10~50

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: MLXIPL Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

Expiry Date: 6 months

Target Details for MLXIPL

Target: MLXIPL (MLX Interacting Protein-Like (MLXIPL))

Alternative Name: MLXIPL

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.

Molecular Weight: 93073

Gene ID: 51085

NCBI Accession: NP_116569, NP_116570, NP_116571, NP_116572

UniProt: Q9NP71

Pathways: Carbohydrate Homeostasis, Regulation of Carbohydrate Metabolic Process