catalog number :
MBS9363754
products type :
ELISA Kit
products full name :
Mouse Gephyrin (GPHN) ELISA Kit
products short name :
[Gephyrin (GPHN)]
other names :
[gephyrin; Gephyrin; gephyrin; gephyrin; Molybdopterin adenylyltransferase (EC:2.7.7.75); MPT adenylyltransferaseAlternative name(s):Domain G]
products gene name :
[GPHN]
other gene names :
[GPHN; GPHN; GPH; GEPH; HKPX1; GPHRYN; MOCODC; GPH; KIAA1385; MPT adenylyltransferase; MPT Mo-transferase]
uniprot entry name :
GEPH_HUMAN
specificity :
No significant cross-reactivity or interference between this analyte and analogues is observed.
storage stability :
Store all reagents at 2-8 degree C
other info1 :
Samples: Human Body Fluids And Tissue Homogenates. Assay Type: Quantitative Sandwich. Detection Range: 3.12ng/ml-100ng/ml. Sensitivity: 1.0ng/ml.
other info2 :
Intra-assay Precision: Intra-assay CV (%) is less than 15%. Inter-assay Precision: Inter-assay CV (%) is less than 15%. [CV(%) = SD/mean ×100]. All CV% should be compared by concentration, not compared by OD values.
products description :
Background/Introduction: This Quantitative Sandwich ELISA kit is for lab reagent/research use only, not for drug, household, therapeutic or diagnostic applications! This kit is intended to be used for determine the level of GPD1L (hereafter termed "analyte") in undiluted original Human body fluids and tissue homogenates. This kit is NOT suitable for assaying non-biological sources of substances.
ncbi acc num :
AAF81785.1
ncbi mol weight :
83,448 Da
ncbi pathways :
GABAergic Synapse Pathway (377263); GABAergic Synapse Pathway (377129); Metabolism Pathway (1269956); Metabolism Of Vitamins And Cofactors Pathway (1270144); Metabolism Of Water-soluble Vitamins And Cofactors Pathway (1270145); Molybdenum Cofactor Biosynthesis Pathway (1270157); Molybdenum Cofactor Biosynthesis Pathway (545431); Molybdenum Cofactor Biosynthesis Pathway (545283)
ncbi summary :
This gene encodes a neuronal assembly protein that anchors inhibitory neurotransmitter receptors to the postsynaptic cytoskeleton via high affinity binding to a receptor subunit domain and tubulin dimers. In nonneuronal tissues, the encoded protein is also required for molybdenum cofactor biosynthesis. Mutations in this gene may be associated with the neurological condition hyperplexia and also lead to molybdenum cofactor deficiency. Numerous alternatively spliced transcript variants encoding different isoforms have been described; however, the full-length nature of all transcript variants is not currently known. [provided by RefSeq, Jul 2008]
uniprot summary :
gephyrin: Microtubule-associated protein involved in membrane protein-cytoskeleton interactions. It is thought to anchor the inhibitory glycine receptor (GLYR) to subsynaptic microtubules. Catalyzes two steps in the biosynthesis of the molybdenum cofactor. In the first step, molybdopterin is adenylated. Subsequently, molybdate is inserted into adenylated molybdopterin and AMP is released. Homotrimer. Interacts with GABARAP. Inhibited by copper and tungsten. 2 isoforms of the human protein are produced by alternative splicing. Protein type: Adaptor/scaffold; EC 2.10.1.1; EC 2.7.7.75. Chromosomal Location of Human Ortholog: 14q23.3. Cellular Component: cell junction; cytoplasm; cytoskeleton; plasma membrane; postsynaptic membrane. Molecular Function: ATP binding; metal ion binding. Biological Process: establishment of synaptic specificity at neuromuscular junction; Mo-molybdopterin cofactor biosynthetic process; molybdenum incorporation into molybdenum-molybdopterin complex; molybdopterin cofactor biosynthetic process; vitamin metabolic process; water-soluble vitamin metabolic process. Disease: Hyperekplexia, Hereditary 1; Molybdenum Cofactor Deficiency, Complementation Group C
size4 :
10x96-Strip-Wells