ganglioside-induced differentiation-associated protein 1, ELISA Kit

Human Ganglioside-induced differentiation-associated protein 1 (GDAP1) ELISA kit; CMTRIA; ; ganglioside-induced differentiation-associated protein 1

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 GDAP1 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.

MBS9319895 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the ganglioside-induced differentiation-associated protein 1 (GDAP1) 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 GDAP1. The ELISA analytical biochemical technique of the MBS9319895 kit is based on GDAP1 antibody-GDAP1 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect GDAP1 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, GDAP1. 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(%).

41,346 Da

ganglioside induced differentiation associated protein 1

ganglioside-induced differentiation-associated protein 1; Charcot-Marie-Tooth neuropathy 4A; ganglioside differentiation associated protein 1

Ganglioside-induced differentiation-associated protein 1

GDAP1  [Similar Products]

GDAP1_HUMAN

This gene encodes a member of the ganglioside-induced differentiation-associated protein family, which may play a role in a signal transduction pathway during neuronal development. Mutations in this gene have been associated with various forms of Charcot-Marie-Tooth Disease and neuropathy. Two transcript variants encoding different isoforms and a noncoding variant have been identified for this gene. [provided by RefSeq, Feb 2012]

GDAP1: the ganglioside-induced differentiation associated protein-1 gene causes autosomal recessive demyelinating or axonal Charcot-Marie-Tooth neuropathy (CMT).

Protein type: Membrane protein, multi-pass

Chromosomal Location of Human Ortholog: 8q21.11

Cellular Component: membrane; mitochondrion; cytoplasm; nucleus; integral to mitochondrial outer membrane

Biological Process: mitochondrial fission; response to retinoic acid; protein targeting to mitochondrion

Disease: Charcot-marie-tooth Disease, Axonal, With Vocal Cord Paresis, Autosomal Recessive; Charcot-marie-tooth Disease, Axonal, Type 2k; Charcot-marie-tooth Disease, Type 4a; Charcot-marie-tooth Disease, Recessive Intermediate A

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