Human VDAC1 (Non-Selective Voltage-Gated Ion Channel Vdac1) - Recombinant Protein
Beta LifeScience
SKU/CAT #: BLT-08316P

SDS-PAGE analysis of Human VDAC1 (Non-Selective Voltage-Gated Ion Channel Vdac1) - Recombinant Protein, CAT# BLT-08316P, showing >90% purity under 15% SDS-PAGE (Reduced)
Human VDAC1 (Non-Selective Voltage-Gated Ion Channel Vdac1) - Recombinant Protein
Beta LifeScience
SKU/CAT #: BLT-08316P
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Quantity Pricing
Pack Size | Price (USD) |
---|---|
500 µg | $1,375 |
1 mg | $2,245 |
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Product Overview
Product Name | Recombinant Human Voltage Dependent Anion Channel 1 (VDAC1) Protein |
Product Overview | This recombinant human Voltage Dependent Anion Channel 1 (VDAC1) protein includes amino acids 2-283aa of the target gene is expressed in E.coli.The protein is supplied in lyophilized form and formulated in PBSprior to lyophilization. |
Target Uniprot Id | P21796 |
Recommended Name | Non-selective voltage-gated ion channel VDAC1 |
Gene Name | VDAC1 |
Synonyms | PORIN-31-HL; Porin 31HM; Plasmalemmal porin; Outer mitochondrial membrane protein porin 1; Voltage-d |
Species | Human |
Predicted Molecular Mass | 61 kDa |
Expression System | E.coli |
Expression Range | 2-283aa |
Tag | N-6His+GST |
Purity | >90% |
Formulation | Lyophilized |
Buffer | PBS |
Storage Condition | 1. Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. 2. Avoid repeated freeze-thaw cycles. 3. Store working aliquots at 4°C for up to one week. 4. In general, protein in liquid form is stable for up to 6 months at -20°C/-80°C. Protein in lyophilized powder form is stable for up to 12 months at -20°C/-80°C. |
Reconstitution Instruction | Briefly centrifuged the vial prior to opening to bring the contents to the bottom. Reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL. It is recommended to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20°C/-80°C. The default final concentration of glycerol is 50%. |
Applications | Positive Control; Immunogen; SDS-PAGE; WB |
Research Area | Cancer |
Target Function | Forms 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. Binds various signaling molecules, including the sphingolipid ceramide, the phospholipid phosphatidylcholine, and the sterol cholesterol. 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. May participate in the formation of the permeability transition pore complex (PTPC) responsible for the release of mitochondrial products that triggers apoptosis. May mediate ATP export from cells. |
Subcellular Location | Mitochondrion outer membrane; Multi-pass membrane protein. Cell membrane; Multi-pass membrane protein. Membrane raft; Multi-pass membrane protein. |
Protein Family | Eukaryotic mitochondrial porin family |
Tissue Specificity | Expressed in erythrocytes (at protein level). Expressed in heart, liver and skeletal muscle. |