GPD2 Recombinant Rabbit Monoclonal Antibody [PSH0-31] - BSA and Azide free
Catalog# HA750605
GPD2 Recombinant Rabbit Monoclonal Antibody [PSH0-31] - BSA and Azide free
-
WB
-
FC
-
Human
-
unconjugated
Overview
Product Name
GPD2 Recombinant Rabbit Monoclonal Antibody [PSH0-31] - BSA and Azide free
Antibody Type
Recombinant Rabbit monoclonal Antibody
Immunogen
Recombinant protein within Human GPD2 aa 43-727.
Species Reactivity
Human
Validated Applications
WB, FC
Target Molecular Weight
Predicted band size: 81 kDa
Positive Control
MCF-7 cell lysate, THP-1 cell lysate, U87-MG cell lysate, HeLa cell lysate, Hela cell.
Conjugation
unconjugated
Clone Number
PSH0-31
Product Features
Form
Liquid
Concentration
1mg/ml
Storage Instructions
Store at 2-8℃. Avoid freeze.
Storage Buffer
1*PBS (pH7.4).
Isotype
IgG
Purification Method
Protein A affinity purified.
Application Dilution
Target
Function
Mitochondrial glycerol-3-phosphate dehydrogenase (GPD2), catalyzes the irreversible oxidation of glycerol-3-phosphate to dihydroxyacetone phosphate and concomitantly transfers two electrons from FAD to the electron transport chain. GPD2 consists of 4 identical subunits. Studies indicate that GPDH is mostly unaffected by pH changes: neither GPD1 or GPD2 is favored under certain pH conditions. At high salt concentrations (E.g. NaCl), GPD1 activity is enhanced over GPD2, since an increase in the salinity of the medium leads to an accumulation of glycerol in response. Changes in temperature do not appear to favor neither GPD1 nor GPD2. The fundamental role of GPDH in maintaining the NAD+/NADH potential, as well as its role in lipid metabolism, makes GPDH a factor in lipid imbalance diseases, such as obesity. Enhanced GPDH activity, particularly GPD2, leads to an increase in glycerol production. Since glycerol is a main subunit in lipid metabolism, its abundance can easily lead to an increase in triglyceride accumulation at a cellular level. As a result, there is a tendency to form adipose tissue leading to an accumulation of fat that favors obesity. GPDH has also been found to play a role in Brugada syndrome. Mutations in the gene encoding GPD1 have been proven to cause defects in the electron transport chain. This conflict with NAD+/NADH levels in the cell is believed to contribute to defects in cardiac sodium ion channel regulation and can lead to a lethal arrythmia during infancy.
Background References
1. Novials A. et al. 1997 Mutation in the calcium-binding domain of the mitochondrial glycerophosphate dehydrogenase gene in a family of diabetic subjects. Biochem Biophys Res Commun. Feb 24;231(3):570-2.
2. Kota V, Dhople VM, Shivaji S (Apr 2009). "Tyrosine phosphoproteome of hamster spermatozoa: role of glycerol-3-phosphate dehydrogenase 2 in sperm capacitation". Proteomics. 9 (7): 1809–26.
Subcellular Location
Mitochondrion.
UNIPROT
Synonyms
GDH2 antibody
Glycerol 3 phosphate dehydrogenase 2 (mitochondrial) antibody
Glycerol 3 phosphate dehydrogenase 2 antibody
Glycerol 3 phosphate dehydrogenase mitochondrial antibody
Glycerol-3-phosphate dehydrogenase antibody
GPD 2 antibody
GPD M antibody
GPD-M antibody
gpd2 antibody
GPDH M antibody
ExpandImages
-
This data was developed using HA721311, the same antibody clone in a different buffer formulation.
Western blot analysis of GPD2 on different lysates with Rabbit anti-GPD2 antibody (HA721311) at 1/1,000 dilution.
Lane 1: MCF-7 cell lysate
Lane 2: THP-1 cell lysate
Lane 3: U87-MG cell lysate
Lane 4: HeLa cell lysate
Lysates/proteins at 10 µg/Lane.
Predicted band size: 81 kDa
Observed band size: 68 kDa
Exposure time: 10s;
10% SDS-PAGE gel.
Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA721311) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:200,000 dilution was used for 1 hour at room temperature. -
This data was developed using HA721311, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of Hela cells labeling GPD2.
Cells were fixed and permeabilized. Then stained with the primary antibody (HA721311, 1ug/ml) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"