Glycine Dehydrogenase (GLDC) ELISA Kits

Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein . Additionally we are shipping Glycine Dehydrogenase Antibodies (62) and Glycine Dehydrogenase Proteins (8) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
GLDC 104174 Q91W43
GLDC 2731 P23378
GLDC 309312  
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Top Glycine Dehydrogenase ELISA Kits at antibodies-online.com

Showing 5 out of 23 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Supplier Delivery Price Details
Mouse 0.063 ng/mL 0.156-10 ng/mL 96 Tests Log in to see 15 to 17 Days
$929.89
Details
Human 4.7 pg/mL 13.7-10.000 pg/mL 96 Tests Log in to see 13 to 16 Days
$707.37
Details
Rat 0.053 ng/mL 0.156-10 ng/mL   96 Tests Log in to see 15 to 17 Days
$973.11
Details
Chicken
  96 Tests Log in to see 15 to 18 Days
$1,095.60
Details
Human
13.72-10000 pg/mL   96 Tests Log in to see 11 to 18 Days
$1,072.50
Details

More ELISA Kits for Glycine Dehydrogenase Interaction Partners

Mouse (Murine) Glycine Dehydrogenase (GLDC) interaction partners

  1. Exencephaly and ventriculomegaly were detectable by High-frequency ultrasound in homozygous Gldc-deficient mouse embryos indicating this to be an effective tool to study CNS development.

  2. These studies support a direct relationship between p53 (show TP53 ELISA Kits) mutations and GLDC expression in B cell lymphoma.

  3. Glycine decarboxylase deficiency causes neural tube defects and features of non-ketotic hyperglycinemia in mice through limiting supply of one-carbon units from mitochondrial folate metabolism.

  4. Results suggest that there is a direct correlation between ischemic injury and extracellular glycine concentration maintained by glycine decarboxylase and the glycine cleavage multienzyme system.

Human Glycine Dehydrogenase (GLDC) interaction partners

  1. We show that the combination of GLDC and HIF-1alpha (show HIF1A ELISA Kits) expression is an independent prognostic factor in early-stage lung non-small cell cancer

  2. Data indicate no mutation was found in glycine cleavage system protein-H (show GCSH ELISA Kits) (GCSH (show GCSH ELISA Kits)) and suggest that mutations in both glycine decarboxylase (GLDC) and aminomethyltransferase (AMT (show AMT ELISA Kits)) are the main cause of glycine encephalopathy in Malaysian population.

  3. study reports a novel mutation, c.2296G>T (p.Gly766Cys), in exon 19 of the glycine decarboxylase (GLDC) gene in a consanguineous Indian couple with a history of 4 neonatal deaths

  4. Identification of a splice acceptor site mutation and five different non-synonymous variants in GLDC were found in patients with neural tube defects.

  5. Study shows that glycine metabolism and the metabolic enzyme glycine decarboxylase (GLDC) drive tumor-initiating cells and tumorigenesis in non-small cell lung cancer.

  6. Heterozygous GLDC gene mutation in transient neonatal hyperglycinemia.

  7. Three adults with mild hyperglycinemia, infantile hypotonia, mental retardation, behavioral hyperirritability, and aggressive outbursts were screened for glycine decarboxylase mutations; two novel missense mutations were found.

  8. The mutation in this nonketotic hyperglycinemia kindred led to missplicing and reduced GLDC (glycine decarboxylase) expression.

  9. Single nucleotide substitution that abolishes the initiator methionine codon of the GLDC gene is associated with glycine encephalopathy

  10. the nonketotic hyperglycinemia is due to a novel GLDC mutation.

Glycine Dehydrogenase (GLDC) Antigen Profile

Antigen Summary

Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein encoded by this gene is the P protein, which binds to glycine and enables the methylamine group from glycine to be transferred to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH).

Gene names and symbols associated with Glycine Dehydrogenase (GLDC) ELISA Kits

  • glycine dehydrogenase (gcvP) antibody
  • glycine dehydrogenase (Tb927.7.1910) antibody
  • glycine cleavage system P-protein (gcvP) antibody
  • glycine decarboxylase (Gldc) antibody
  • glycine dehydrogenase (decarboxylating) (GLDC) antibody
  • glycine dehydrogenase (decarboxylating) (Gldc) antibody
  • D030049L12Rik antibody
  • D19Wsu57e antibody
  • DDBDRAFT_0219205 antibody
  • DDBDRAFT_0231130 antibody
  • DDB_0219205 antibody
  • DDB_0231130 antibody
  • GCE antibody
  • GCSP antibody
  • HYGN1 antibody
  • PSPTO1276 antibody
  • Tb07.43M14.350 antibody

Protein level used designations for Glycine Dehydrogenase (GLDC) ELISA Kits

glycine dehydrogenase , glycine cleavage system P protein , glycine dehydrogenase [decarboxylating], mitochondrial , glycine cleavage system protein P , glycine decarboxylase P-protein , glycine cleavage system protein P) , glycine decarboxylase , glycine dehydrogenase (decarboxylating; glycine decarboxylase, glycine cleavage system protein P) , glycine decarboxylase, glycine cleavage system protein P)

GENE ID SPECIES
1168636 Shewanella oneidensis MR-1
1182912 Pseudomonas syringae pv. tomato str. DC3000
3196586 Ruegeria pomeroyi DSS-3
3658401 Trypanosoma brucei brucei strain 927/4 GUTat10.1
8626028 Dictyostelium discoideum AX4
104174 Mus musculus
2731 Homo sapiens
374222 Gallus gallus
481534 Canis lupus familiaris
309312 Rattus norvegicus
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