VPS13C Antibodies

AND VPS13C ELISA kits, VPS13C Proteins

Many biological assays use antibodies to detect VPS13C, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with VPS13C in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop VPS13C antibodies...

We validate the specificity of these antibodies to VPS13C by testing them on tissues known to express VPS13C positively and negatively. Browse below to find the VPS13C antibody that suites your experiment. We have 1 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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VPS13C Infographic by Boster Bio

All VPS13C Products

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Anti-VPS13C Antibody

Human, Mouse, Rat

ELISA, IHC, WB

$370
Cat # A07275
100 μl/vial

VPS13C Overview

Facts about Vacuolar protein sorting-associated protein 13C.

Vacuolar protein sorting-associated protein 13C (VPS13C)

Necessary for proper mitochondrial function and maintenance of mitochondrial transmembrane potential. Involved in the regulation of PINK1/PRKN-mediated mitophagy in response to mitochondrial depolarization.

Gene Information

Human
Gene Name:	VPS13C
Uniprot:	Q709C8
Entrez:	54832

Family

Belongs to:

VPS13 family

Alternative Names

Vacuolar protein sorting-associated protein 13C

Molecular Weight

Mass (kDA):
422.39 kDA

Genomic Context


Human

Location:	15q22.2
Sequence:	15; NC_000015.10 (61852389..62060465, complement)

Tissue Specificity

Widely expressed.

Subcellular Localizations

Mitochondrion outer membrane.

PTMs

Acetylation

Methylation

Phosphoprotein

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/VPS13C

References

PMID: 15498460 by Velayos-Baeza A., et al. Analysis of the human VPS13 gene family.

PMID: 26942284 by Lesage S., et al. Loss of mitochondrial morphology, transmembrane potential, and respiration function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy.