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 (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). Zusätzlich bieten wir Ihnen Glycine Dehydrogenase Antikörper (63) und Glycine Dehydrogenase Proteine (8) und viele weitere Produktgruppen zu diesem Protein an.

list all ELISA KIts Gen GeneID UniProt
GLDC 104174 Q91W43
GLDC 2731 P23378
GLDC 309312  
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Top Glycine Dehydrogenase ELISA Kits auf antikoerper-online.de

Showing 5 out of 27 products:

Katalog Nr. Reaktivität Sensitivität Bereich Bilder Menge Anbieter Lieferzeit Preis Details
Maus 0.063 ng/mL 0.15 ng/mL - 10 ng/mL 96 Tests Anmelden zum Anzeigen 13 bis 16 Tage
$606.32
Details
Human 4.7 pg/mL 13.7 pg/mL - 10000 pg/mL 96 Tests Anmelden zum Anzeigen 13 bis 16 Tage
$707.37
Details
Ratte 0.053 ng/mL 0.15 ng/mL - 10 ng/mL 96 Tests Anmelden zum Anzeigen 13 bis 16 Tage
$640.00
Details
Huhn
  96 Tests Anmelden zum Anzeigen 15 bis 18 Tage
$1,095.60
Details
Human
13.72-10000 pg/mL   96 Tests Anmelden zum Anzeigen 11 bis 18 Tage
$980.73
Details

Weitere ELISA Kits für Glycine Dehydrogenase Interaktionspartner

Mouse (Murine) Glycine Dehydrogenase (GLDC) Interaktionspartner

  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 (zeige 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) Interaktionspartner

  1. The position and frequency of the breakpoint for CNVs correlated with intron size and presence of Alu elements. Missense mutations, most often recurring, were the most common type of disease-causing mutation in AMT (zeige AMT ELISA Kits)

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

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

  4. 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

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

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

  7. Heterozygous GLDC gene mutation in transient neonatal hyperglycinemia.

  8. 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.

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

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

Glycine Dehydrogenase (GLDC) Antigen-Profil

Beschreibung des Gens

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).

Genbezeichner und Symbole assoziert mit Glycine Dehydrogenase (GLDC) ELISA Kits

  • glycine dehydrogenase (decarboxylating) GcvP (gcvP) Antikörper
  • glycine dehydrogenase (gcvP) Antikörper
  • glycine dehydrogenase (Tb927.7.1910) Antikörper
  • glycine cleavage system P-protein (gcvP) Antikörper
  • glycine decarboxylase (Gldc) Antikörper
  • glycine decarboxylase (GLDC) Antikörper
  • glycine dehydrogenase (decarboxylating) (gldc) Antikörper
  • glycine decarboxylase S homeolog (gldc.S) Antikörper
  • D030049L12Rik Antikörper
  • D19Wsu57e Antikörper
  • DDBDRAFT_0219205 Antikörper
  • DDBDRAFT_0231130 Antikörper
  • DDB_0219205 Antikörper
  • DDB_0231130 Antikörper
  • fb23b05 Antikörper
  • GCE Antikörper
  • GCSP Antikörper
  • gldc Antikörper
  • HYGN1 Antikörper
  • PSPTO1276 Antikörper
  • Tb07.43M14.350 Antikörper
  • wu:fb23b05 Antikörper
  • zgc:66198 Antikörper

Bezeichner auf Proteinebene für Glycine Dehydrogenase (GLDC) ELISA Kits

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GENE ID SPEZIES
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
309312 Rattus norvegicus
481534 Canis lupus familiaris
321621 Danio rerio
379833 Xenopus laevis
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