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VDAC/Porin Antibody

Catalogue number:
600-101-HB2
Size:
100 µg
Product is available in:
  • UK
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Applications:

ELISA, Immunohistochemistry, IF Microscopy, Western Blot

Antibody Host:

Goat

Species Reactivity:

H. sapiens (Human); Mus musculus (Mouse); Rat

Antibody Isotype:

IgG

Antibody Type:

Polyclonal

Immunogen:

VDAC/Porin Antibody was prepared from whole goat serum produced by repeated immunizations with a synthetic peptide corresponding to N-terminal portion

Alternative Names:

Goat anti-VDAC/Porin antibody, VDAC-1 Loading Control Antibody, Porin Loading Control Antibody, VDAC-1 Antibody, VDAC1 Antibody, POR1 Antibody, Porin Antibody, Voltage-dependent anion-selective channel protein 1, Outer mitochondrial membrane protein porin

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Product Description:

VDAC/Porin Antibody recognizes VDAC (also known as Voltage-dependent anion-selective channel protein 1) which is an outer membrane mitochondrial protein. The VDAC proteins are ~30-33 kDa (some isoforms are larger) . The VDAC proteins are thought to form aqueous channels, or pores, through which adenine nucleotides cross the outer mitochondrial membrane. VDACs have been implicated in the formation of the mitochondrial permeability transition pore complex in apoptotic cells. This complex, formed by VDAC, adenine nucleotide translocator (ANT) , and cyclophilin D (CypD) , is thought to allow the mitochondria to undergo metabolic uncoupling and irreversible morphologic changes that ultimately destroy the mitochondria during apoptosis. VDACs are highly expressed in heart, liver and skeletal muscle, where concentrations of mitochondria are at their highest. Diseases associated with VDAC1 include Cystic Fibrosis and Gerstmann-Straussler Disease. This antibody can be used as a loading control with whole cell lysates and total mitochondrial preparations. Anti-VDAC/Porin Antibody is useful for researchers interested in Apoptosis, cell survival and regulation, Mitochondrial Proteins, and Neuroscience Research. VDAC/Porin Antibody has been tested for use in ELISA, western blot, and Immunofluorescence. Specific conditions for reactivity should be optimized by the end user. Expect a band at ~30-33 kDa in size corresponding to VDAC/Porin by western blotting in the appropriate cell lysate or extract. Positive control used in WB: HeLa Whole Cell, Mouse Heart Lysate, or Rat Brain Tissue Lysate, and HeLa Cells in IF.

Immunofluorescence of Goat Anti-VDAC/Por
Immunofluorescence of Goat Anti-VDAC/Porin Antibody. Cell Line: HeLa Cells. Fixation: 100% MeOH. Permeabilization: 0.3% Triton X-100. Primary Antibody: Anti-VDAC1/Porin at 5µg/mL overnight at 2-8°C. Secondary Antibody: Donkey Anti-Goat IgG DyLight™488 (p/n 605-741-125) at 15µg/mL for 1hr at RT. Nuclear counter stain: DAPI. Location: Mitochondrion, Mitochondrion Outer Membrane, Nucleus. A). DAPI. B). VDAC/DyLight™488. C). Merge of A+B. D). Secondary Only.
Western Blot of Goat Anti-VDAC/Porin Ant
Western Blot of Goat Anti-VDAC/Porin Antibody. Lane 1: PreStained Molecular weight (p/n MB-210-0500). Lane 2: full length recombinant human VDAC1 GST-tag. Lane 3: HeLa Whole Cell Lysate (p/n W09-000-364). Lane 4: Rat Brain Lysate (p/n W12-000-T077). Load: 10µg. Primary Antibody: Anti-VDAC/Porin at 1µg/mL overnight at 2-8°C. Secondary Antibody: F(ab')2 Anti-GOAT IgG (p/n 705-703-125) at 1:70,000 for 30min at RT. Blocking buffer: BlockOut (p/n MB-073). Expect: ~62kDa recombinant/~33kDa endogenous. Observed: ~57kDa recombinant/~33kDa endogenous.