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R2556-vp - MLXIPL (vPairTM) Antibodies
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Uniprot ID: Q99MZ3 Application: WB, IP, ChIP Predicted I Observed M.W.: 95 I 120 kDa Quantity: 50 ul MLXIPL (N2) (R2556-2) Rabbit Polyclonal Antibody & 50 ul MLXIPL (C) (R2556-3) Rabbit Polyclonal Antibody Product Introduction: vPairTM antibodies represent a pair of fully characterized antibodies that recognize two different regions of a target protein. The product is developed by Abiocode to address whether the signal observed truly represents the protein of interest, an often encountered issue in antibody-based assays. The use of a pair of fully characterized vPairTM antibodies in the same assay can validate signal specificity since vPairTM antibodies recognize two independent epitopes of the same protein. Different sets of vPairTM antibodies are developed at Abiocode to work with specific applications, including antibody arrays, Western blot, IP-Western, ChIP, IHC, and FACS. Background: MLX-interacting protein-like (MLXIPL) is a nuclear protein involved in transcriptional regulation. MLXIPL contains 1 basic helix-loop-helix (bHLH) domain and binds to the canonical and non-canonical E box sequences 5'-CACGTG-3'. MLXIPL is a transcriptional repressor. Other Names: Carbohydrate-responsive element-binding protein, ChREBP, MLX interactor, MLX-interacting protein-like, Williams-Beuren syndrome chromosomal region 14 protein homolog, Mio, Wbscr14 Source and Purity: Rabbit polyclonal antibodies were produced by immunizing animals with GST-fusion proteins containing either the N-terminal [MLXIPL (N2) (R2556-2)] or the C-terminal [MLXIPL (C) (R2556-3)] region of mouse MLXIPL. Antibodies were purified by affinity purification using immunogen. Storage Buffer and Condition: Supplied in 1 x PBS (pH 7.4), 100 ug/ml BSA, 40% Glycerol, 0.01% NaN3. Store at -20 °C. Stable for 6 months from date of receipt. Species Specificity: Human, Mouse Tested Applications: WB: 1:1,000-1:3,000 (detect endogenous protein*)
IP & ChIP: 1:100-1:200
*: The apparent protein size on WB may be different from the calculated M.W. due to modifications. Product Data: Fig 1. (A) Western blot (WB) of total cell extracts from (a,c) human HeLa, (b,d) human Jurkat, (e) human HepG2; using 2 independent Abs against 2 distinct regions of mouse MLXIPL at RT for 2 h. (B) IP-WB. Immunoprecipitaion (IP) was performed with HeLa or Jurkat extracts with IgG or anti-MLXIPL (C) (R2556-3) as indicated, followed by WB with anti-MLXIPL (N2) (R2556-2). (C) Total extracts from human HepG2 were immunoprecipitated with IgG or anti-MLXIPL (C) (R2556-3) under the conventional IP conditions or cross-linked chromatin immunoprecipitation (ChIP) conditions; followed by WB with anti-MLXIPL (N2) (R2556-2) at RT for 2 h. |