Cell Signaling Technology

Product Pathways - Cytoskeletal Signaling

VDAC Antibody #4866

Applications Reactivity Sensitivity MW (kDa) Source
W IHC-P H M R B Endogenous 32 Rabbit

Applications Key:  W=Western Blotting  IHC-P=Immunohistochemistry (Paraffin)
Reactivity Key:  H=Human  M=Mouse  R=Rat  B=Bovine
Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

Protocols

Specificity / Sensitivity

VDAC Antibody detects endogenous levels of total VDAC protein.

Source / Purification

Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to the amino terminus of human VDAC-1. Antibodies are purified using protein A and peptide affinity chromatography.

Western Blotting

Western Blotting

Western blot analysis of extracts from various cell lines, using VDAC Antibody.

IHC-P (paraffin)

IHC-P (paraffin)

Immunohistochemical analysis of paraffin-embedded human breast carcinoma, using VDAC Antibody.

IHC-P (paraffin)

IHC-P (paraffin)

Immunohistochemical analysis of paraffin-embedded human colon carcinoma, using VDAC Antibody.


IHC-P (paraffin)

IHC-P (paraffin)

Immunohistochemical analysis of paraffin-embedded 4T1 syngeneic mouse tumor using VDAC Antibody.

IHC-P (paraffin)

IHC-P (paraffin)

Immunohistochemical analysis of paraffin-embedded human breast carcinoma, using VDAC Antibody in the presence of control peptide (left) or antigen-specific peptide (right).

Background

Voltage-dependent anion channel (VDAC), ubiquitously expressed and located in the outer mitochondrial membrane, is generally thought to be the primary means by which metabolites diffuse in and out of the mitochondria (1). In addition, this channel plays a role in apoptotic signaling. The change in mitochondrial permeability characteristic of apoptosis is mediated by Bcl-2 family proteins, which bind to VDAC, altering the channel kinetics (2). Homodimerization of VDAC may be a mechanism for changing mitochondrial permeability and supporting release of cytochrome c (3). In mammalian cells, there are three VDAC isoforms, VDAC1, which is the most widely expressed isoform, as well as VDAC2 and VDAC3 (4,5).

  1. Hodge, T. and Colombini, M. (1997) J Membr Biol 157, 271-9.
  2. Shimizu, S. et al. (1999) Nature 399, 483-7.
  3. Zheng, Y. et al. (2004) Oncogene 23, 1239-47.
  4. Craigen, W.J. and Graham, B.H. (2008) J Bioenerg Biomembr 40, 207-12.
  5. Yamamoto, T. et al. (2006) J Proteome Res 5, 3336-44.

Application References

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Companion Products


For Research Use Only. Not For Use In Diagnostic Procedures.

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