vacuolar protein sorting 13 homolog B (yeast), ELISA Kit

Human Vacuolar protein sorting-associated protein 13B (VPS13B) ELISA kit; CHS1; COH1; DKFZp313I0811; KIAA0532; Cohen syndrome 1; vacuolar protein sorting 13B; vacuolar protein sorting 13 homolog B (yeast)

For Research Use Only. Not for use in diagnostic procedures.

Store all reagents at 2-8 degree C

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Small volumes of VPS13B elisa kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

MBS9335589 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the vacuolar protein sorting 13 homolog B (yeast) (VPS13B) ELISA Kit target analytes in biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing VPS13B. The ELISA analytical biochemical technique of the MBS9335589 kit is based on VPS13B antibody-VPS13B antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect VPS13B antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, VPS13B. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).

448,664 Da

vacuolar protein sorting 13 homolog B (yeast)

vacuolar protein sorting-associated protein 13B

Vacuolar protein sorting-associated protein 13B

CHS1; COH1; KIAA0532  [Similar Products]

VP13B_HUMAN

This gene encodes a potential transmembrane protein that may function in vesicle-mediated transport and sorting of proteins within the cell. This protein may play a role in the development and the function of the eye, hematological system, and central nervous system. Mutations in this gene have been associated with Cohen syndrome. Multiple splice variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]

VPS13B: May be involved in protein sorting in post Golgi membrane traffic. Defects in VPS13B are a cause of Cohen syndrome (COH1). COH1 is a rare autosomal recessive disorder characterized by obesity, hypotonia, intellectual deficit, characteristic craniofacial dysmorphism and abnormalities of the hands and feet. Characteristic facial features include high-arched or wave-shaped eyelids, a short philtrum, thick hair and low hairline. Belongs to the VPS13 family. 6 isoforms of the human protein are produced by alternative splicing.

Protein type: Vesicle; Membrane protein, integral

Chromosomal Location of Human Ortholog: 8q22.2

Biological Process: protein transport

Disease: Cohen Syndrome

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