Goat Anti-VPS35 / MEM3 Antibody

This goat IgG polyclonal antibody was generated against peptide sequence CSPESEGPIYEGLIL from the C Terminus of vacuolar protein sorting-associated protein 35 (VPS35) and recognizes human, mouse, and rat VPS35.

Highlights:

  • Reacts with human, mouse, and rat VPS35
  • Suitable for Peptide ELISA, Western Blot, Immunohistochemistry, and Immunofluorescence applications
  • Parkinson disease 17 and hereditary late-onset Parkinson disease are associated with mutations in the VPS35 gene.

Vacuolar protein sorting-associated protein 35 (VPS35) is a component of a multimeric complex termed the retromer cargo-selective complex (CSC). In addition to VPS35, the CSC is comprised of two other proteins, VPS26 and Vps29. The CSC is involved in the retrograde transport of cargo proteins from endosomes to the trans-Golgi network predominantly via VPS35. Mutations in the VPS35 gene are associated with Parkinson disease 17 and hereditary late-onset Parkinson disease.

Catalog Number Product DataSheet Size AVAILABILITY Price Qty
EB06268
Goat Anti-VPS35 / MEM3 Antibody
100ug specific antibody in 200ul In stock
Regular Price:$415.00
On Sale:
Specifications

Product Type: Antibody
Name: Goat Anti-VPS35 / MEM3 Antibody
Alternative Name(s): MEM3, PARK17
Accession ID: NP_060676.2
Antigen: VPS35 / MEM3
Isotype: IgG
Clonality: Polyclonal
Reactivity: Human, Mouse, Rat
Specificity: VPS35 / MEM3
Immunogen: CSPESEGPIYEGLIL
Species Immunized: Goat
Epitope: C Terminus
Purification Method: Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide
Buffer: Supplied at 0.5 mg/ml in Tris saline, 0.02% sodium azide, pH7.3 with 0.5% bovine serum albumin.
Tested Applications: Pep-ELISA, WB, IHC, IF
Storage: Aliquot and store at -20C. Minimize freezing and thawing.
Shipped: Cold Packs

Documentation
Data

Western Blot, Immunofluorescence, and Immunohistochemistry

WB Data

I. (0.03µg/ml) staining of Human (A) Mouse (B) and Rat (C) Brain lysate (35µg protein in RIPA buffer). Detected by chemiluminescence. II. (0.03µg/ml) staining of HepG2 (A) and HEK293 (B) cell lysate (35µg protein in RIPA buffer). Detected by chemiluminescence. III. Immunofluorescence analysis of paraformaldehyde fixed HEK293 cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing cytoplasmic/vesicle staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml). IV. Immunofluorescence analysis of paraformaldehyde fixed U2OS cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing cytoplasmic/vesicle staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml). V. (8µg/ml) staining of paraffin embedded Human Prostate. Heat induced antigen retrieval with citrate buffer pH 6, HRP-staining. VI. Negative control showing staining of paraffin embedded Human Prostate with no primary antibody.

References
  1. Lee S, Uchida Y, Emoto K, Umeda M, Kuge O, Taguchi T, Arai H., Impaired retrograde membrane traffic through endosomes in a mutant CHO cell defective in phosphatidylserine synthesis., Genes Cells. 2012 Aug;17(8):728-36. doi: 10.1111/j.1365-2443.2012.01622.x. ,22747682

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