Glycine Dehydrogenase (GLDC) ELISA试剂盒

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). 再加上,我们可以发Glycine Dehydrogenase 抗体 (63)Glycine Dehydrogenase 蛋白 (8)和数多这个蛋白质的别的产品。

list all ELISA KIts 基因 基因ID UniProt
GLDC 104174 Q91W43
GLDC 2731 P23378
GLDC 309312  
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Showing 8 out of 27 products:

产品编号 适用 灵敏度 范围 图像 规格 供应商 交付 价格 详细
小鼠 0.063 ng/mL 0.15 ng/mL - 10 ng/mL 96 Tests Log in to see 13至16个工作日
$606.32
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4.7 pg/mL 13.7 pg/mL - 10000 pg/mL 96 Tests Log in to see 13至16个工作日
$707.37
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大鼠 0.053 ng/mL 0.15 ng/mL - 10 ng/mL 96 Tests Log in to see 13至16个工作日
$640.00
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0.132 ng/mL 0.312 ng/mL - 20 ng/mL   96 Tests Log in to see 8至12个工作日
$766.25
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小鼠 0.063 ng/mL 0.156 ng/mL - 10 ng/mL   96 Tests Log in to see 8至12个工作日
$787.25
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大鼠 0.053 ng/mL 0.156 ng/mL - 10 ng/mL   96 Tests Log in to see 8至12个工作日
$829.25
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小鸡
  96 Tests Log in to see 15至18个工作日
$1,095.60
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13.72-10000 pg/mL   96 Tests Log in to see 11至18个工作日
$980.73
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适于 Glycine Dehydrogenase 相互作用对的更多 ELISA 试剂盒

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 (显示 TP53 ELISA试剂盒) 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. 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 (显示 AMT ELISA试剂盒)

  2. We show that the combination of GLDC and HIF-1alpha (显示 HIF1A ELISA试剂盒) 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 (显示 GCSH ELISA试剂盒) (GCSH (显示 GCSH ELISA试剂盒)) and suggest that mutations in both glycine decarboxylase (GLDC) and aminomethyltransferase (AMT (显示 AMT ELISA试剂盒)) 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) 抗原简介

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 GLDC

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

Protein level used designations for GLDC

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) , glycine dehydrogenase (decarboxylating), mitochondrial , glycine decarboxylase S homeolog , glycine dehydrogenase (decarboxylating) S homeolog

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