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Rabbit Anti-MPC1 Recombinant Antibody (D2L9I) (CBMAB-CP0033-LY)

The product is antibody recognizes MPC1. The antibody D2L9I immunoassay techniques such as: WB,IP.
See all MPC1 antibodies

Summary

Host Animal
Rabbit
Specificity
Human, Mouse, Rat, Monkey
Clone
D2L9I
Antibody Isotype
IgG
Application
WB, IP

Basic Information

Immunogen
Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues near the carboxy terminus of human MPC1 protein.
Specificity
Human, Mouse, Rat, Monkey
Antibody Isotype
IgG
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
100 µg/ml BSA, 50% glycerol
Preservative
0.02% sodium azide
Purity
> 95% Purity determined by SDS-PAGE.
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freezethaw cycles.

Target

Full Name
Mitochondrial Pyruvate Carrier 1
Introduction
The protein encoded by this gene is part of an MPC1/MPC2 heterodimer that is responsible for transporting pyruvate into mitochondria. The encoded protein is found in the inner mitochondrial membrane. Defects in this gene are a cause of mitochondrial pyruvate carrier deficiency. Several transcript variants, some protein coding and one non-protein coding, have been found for this gene. [provided by RefSeq, Aug 2012]
Entrez Gene ID
Human51660
Mouse55951
Rat171087
Monkey716864
UniProt ID
HumanQ9Y5U8
MouseP63030
RatP63031
MonkeyH9EW80
Alternative Names
Mitochondrial Pyruvate Carrier 1; Brain Protein 44-Like Protein; BRP44L; Brain Protein 44-Like; HSPC040 Protein; DJ68L15.3; CGI-129; SLC54A1; MPYCD;
Function
Mediates the uptake of pyruvate into mitochondria.
Biological Process
Mitochondrial pyruvate transmembrane transport Source: GO_Central
Cellular Location
Mitochondrion inner membrane
Involvement in disease
Mitochondrial pyruvate carrier deficiency (MPYCD):
An autosomal recessive metabolic disorder characterized by severely delayed psychomotor development, mild dysmorphic features, hepatomegaly, marked metabolic acidosis, hyperlactacidemia with normal lactate/pyruvate, and encephalopathy. Some patients have epilepsy and peripheral neuropathy.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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