Antibody Details
Product Details
ImmunogenFusion protein corresponding to aa 1-283 (full-length) of human VDAC1. This sequence is 98
FormulationPBS, pH 7.4, 0.1% sodium azide, 50% glycerol.
Product PreparationPurified by Protein G affinity chromatography
Storage and HandlingThis product is stable for at least one (1) year at -20°C.
Regulatory StatusFor in vitro investigational use only. Not intended for therapeutic or diagnostic procedures.
Applications and Recommended Usage?
Quality Tested by LeincoImmunoblotting: use at 1-5ug/mL. A band of ~30kDa is detected.
Immunofluorescence: use at 10ug/mL
These are recommended concentrations.
Endusers should determine optimal concentrations for their application.
Each investigator should determine their own optimal working dilution for specific applications. See directions on lot specific datasheets, as information may periodically change.
Description
Description
Specificity This antibody recognizes human, mouse and rat VDAC1. It does not cross-react
with VDAC2 or VDAC3 (based on evaluation in knock-out mice).
BackgroundVDAC1 (also known as Voltage-dependent anion-selective channel protein 1 and outer mitochondrial membrane protein porin 1) is the outer mitochondrial membrane receptor for hexokinase and BCL2L1. VDAC1 forms a channel through the mitochondrial membrane and is involved in small molecule diffusion, cell volume regulation, and apoptosis. VDAC1 may participate in the formation of the permeability transition pore complex (PTPC) which is responsible for the release of mitochondrial products that trigger apoptosis.
FunctionForms a channel through the mitochondrial outer membrane and also the plasma membrane. The channel at the outer mitochondrial membrane allows diffusion of small hydrophilic molecules; in the plasma membrane it is involved in cell volume regulation and apoptosis. It adopts an open conformation at low or zero membrane potential and a closed conformation at potentials above 30-40 mV. The open state has a weak anion selectivity whereas the closed state is cation-selective (PubMed:11845315, PubMed:18755977, PubMed:20230784, PubMed:8420959). Binds various signaling molecules, including the sphingolipid ceramide, the phospholipid phosphatidylcholine, and the sterol cholesterol (PubMed:31015432). In depolarized mitochondria, acts downstream of PRKN and PINK1 to promote mitophagy or prevent apoptosis; polyubiquitination by PRKN promotes mitophagy, while monoubiquitination by PRKN decreases mitochondrial calcium influx which ultimately inhibits apoptosis (PubMed:32047033). May participate in the formation of the permeability transition pore complex (PTPC) responsible for the release of mitochondrial products that triggers apoptosis (PubMed:15033708, PubMed:25296756). May mediate ATP export from cells (PubMed:30061676). {PubMed:11845315, PubMed:15033708, PubMed:18755977, PubMed:20230784, PubMed:25296756, PubMed:30061676, PubMed:31015432, PubMed:32047033, PubMed:8420959}.
References & Citations
Certificate of Analysis