The DLAT Monoclonal Antibody (CAB8814) is a high-quality antibody developed for reliable detection and analysis of target proteins. This antibody, generated in rabbits, is highly specific and validated for use in various applications, including Western blot and immunohistochemistry.DLAT, also known as dihydrolipoamide S-acetyltransferase, plays a crucial role in energy production within the mitochondria by catalyzing the transfer of acetyl groups. Dysregulation of DLAT has been linked to various metabolic disorders, making it an important target for research in areas such as metabolism, diabetes, and mitochondrial diseases.
This antibody is validated for use in WB, ELISA applications and has demonstrated reactivity against Human, Mouse, Rat samples.
Product Name:
DLAT Monoclonal Antibody
SKU:
CAB8814
Size:
20μL, 100μL
Reactivity:
Human, Mouse, Rat
Clone Number:
ARC1314
Conjugate:
Unconjugated
Immunogen:
Synthetic peptide. This information is considered to be commercially sensitive.
Recommended starting concentration is 1 μg/mL. Please optimize the concentration based on your specific assay requirements.
Synonyms:
E2, PBC, DLTA, PDCE2, PDC-E2, DLAT
Positive Sample:
HeLa, Hep G2, MCF7, NIH/3T3, C6, Mouse liver
Cellular Localization:
Mitochondrion Matrix.
Calculated MW:
69kDa
Observed MW:
69kDa
This gene encodes component E2 of the multi-enzyme pyruvate dehydrogenase complex (PDC). PDC resides in the inner mitochondrial membrane and catalyzes the conversion of pyruvate to acetyl coenzyme A. The protein product of this gene, dihydrolipoamide acetyltransferase, accepts acetyl groups formed by the oxidative decarboxylation of pyruvate and transfers them to coenzyme A. Dihydrolipoamide acetyltransferase is the antigen for antimitochondrial antibodies. These autoantibodies are present in nearly 95% of patients with the autoimmune liver disease primary biliary cirrhosis (PBC). In PBC, activated T lymphocytes attack and destroy epithelial cells in the bile duct where this protein is abnormally distributed and overexpressed. PBC enventually leads to cirrhosis and liver failure. Mutations in this gene are also a cause of pyruvate dehydrogenase E2 deficiency which causes primary lactic acidosis in infancy and early childhood.
Purification Method
Affinity purification
Gene ID
1737
RRID
AB_2863614
Buffer Information
Store at -20℃. Avoid freeze / thaw cycles. Buffer: PBS containing 50% glycerol and 0.05% BSA, preserved with proclin300 or sodium azide, pH 7.3.
Western blot analysis of various lysates using DLAT Rabbit mAb (CAB8814) at 1:1000 dilution. Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution. Lysates/proteins: 25μg per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit (AbGn00020). Exposure time: 1min.
