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Antigenic Specificity | MTTP |
Clone | polyclonal |
Host Species | Rabbit |
Reactive Species | human, mouse, rat |
Isotype | n/a |
Format | immunogen affinity purified |
Size | 0.1 mg |
Concentration | n/a |
Applications | Western Blot (WB), Immunohistochemistry (IHC) Formalin/Paraffin, Flow Cytometry (FC/FACS), Direct ELISA (EIA) |
Reviews / Ratings | If you have used this antibody, please help fellow researchers by submitting reviews to pAbmAbs and antYbuddY. |
Description | Specificity: No cross reactivity with other proteins. Description: Rabbit IgG polyclonal antibody for MTTP detection. Tested with WB, IHC-P, IHC-F, FCM, Direct ELISA in Human; Mouse; Rat.Background: Microsomal triglyceride transfer protein large subunit is a protein that in humans is encoded by the MTTP gene. It is mapped to 4q23. MTP encodes the large subunit of the heterodimeric microsomal triglyceride transfer protein. Protein disulfide isomerase (PDI) completes the heterodimeric microsomal triglyceride transfer protein, which has been shown to play a central role in lipoprotein assembly. Mutations in MTP can cause abetalipoproteinemia. |
Immunogen | Immunogen: E Coli-derived human MTTP recombinant protein (Position: N29-R702). Contents: Each vial contains 4mg Trehalose, 0.9mg NaCl, 0.2mg Na2HPO4, 0.05mg NaN3. Relevant Detection Systems: Relevant Detection Systems: We recommend Enhanced Chemiluminescent Kit with anti-Rabbit IgG (MBS176460) for Western blot, and HRP Conjugated anti-Rabbit IgG Super Vision Assay Kit (MBS176453) for IHC(P), IHC(F) and ICC. |
Other Names | [Microsomal triglyceride transfer protein large subunit; microsomal triglyceride transfer protein; Microsomal triglyceride transfer protein large subunit; MTTP; MTP] |
Gene, Accession # | [MTTP], Gene ID: 4547, NCBI: P55157.1, UniProt: P55157 |
Catalog # | MBS1752472 |
Price | $280 |
Order / More Info | MTTP Antibody from MYBIOSOURCE INC. |
Product Specific References | 1. Al-Shali, K., Wang, J., Rosen, F., Hegele, R. A. Ileal adenocarcinoma in a mild phenotype of abetalipoproteinemia. Clin. Genet. 63: 135-138, 2003. 2. Benayoun, L., Granot, E., Rizel, L., Allon-Shalev, S., Behar, D. M., Ben-Yosef, T. Abetalipoproteinemia in Israel: evidence for a founder mutation in the Ashkenazi Jewish population and a contiguous gene deletion in an Arab patient. Molec. Genet. Metab. 90: 453-457, 2007. |