Methylcrotonoyl-CoA Carboxylase 1 (Alpha) (MCCC1) ELISA试剂盒

MCCC1 encodes the large subunit of 3-methylcrotonyl-CoA carboxylase. 再加上,我们可以发Methylcrotonoyl-CoA Carboxylase 1 (Alpha) 抗体 (36)Methylcrotonoyl-CoA Carboxylase 1 (Alpha) 蛋白 (7)和数多这个蛋白质的别的产品。

list all ELISA KIts 基因 基因ID UniProt
MCCC1 56922 Q96RQ3
大鼠 MCCC1 MCCC1 294972 Q5I0C3
小鼠 MCCC1 MCCC1 72039 Q99MR8
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产品编号 适用 灵敏度 范围 图像 规格 供应商 交付 价格 详细
5.8 pg/mL 23.5-1500 pg/mL Typical standard curve 96 Tests Log in to see 15至18个工作日

适于 Methylcrotonoyl-CoA Carboxylase 1 (Alpha) 相互作用对的更多 ELISA 试剂盒

Human Methylcrotonoyl-CoA Carboxylase 1 (Alpha) (MCCC1) interaction partners

  1. This study reports data mainly obtained from the Portuguese newborn screening program collected over a ten-year period. Analysis of the MCCC1 and MCCC2 (显示 MCCC2 ELISA试剂盒) genes yielded 26 previously unreported mutations and a variant of clinically unknown significance.

  2. Our study provides strong support for the susceptibility role of RAB7L1/NUCKS1 rs823118 and MCCC1 rs12637471 in sporadic Parkinson's disease in a Han Chinese population

  3. Novel mutations in MCCC1 gene were identified in Chinese population. The expression profiles of two splice mutations (c.639+2T>A and c.639+5G>T) were also characterized.

  4. Four new point mutations were detected in the MCCC1 gene in patients with maternal 3-methylcrotonyl coenzyme deficiency.

  5. This study demonistrated that Mainland China demonstrates that MCCC1/LAMP3 (rs11711441) is associated with a lower risk of Parkinson's disease.

  6. 3-methylcrotonyl-CoA carboxylase (显示 MCCC2 ELISA试剂盒) inhibition has a role in increased excretion of 3-hydroxyisovaleric acid in valproate-treated patients

  7. Mutation in 3-methylcrotonyl CoA carboxylase 1 gene is associated with 3-methylcrotonyl-CoA carboxylase (显示 MCCC2 ELISA试剂盒) deficiency.

  8. study reports eight different mutant alleles of MCCC1 or MCCC2 including six novel mutations in Korean patients with 3-methylcrotonyl-CoA carboxylase (MCC) deficiency

  9. identified two novel MCCA and four novel MCCB mutant alleles from five MCC-deficient patients

  10. factors other than the genotype at the MCCA and MCCB loci have a major influence on the phenotype of MCC deficiency

Arabidopsis thaliana Methylcrotonoyl-CoA Carboxylase 1 (Alpha) (MCCC1) interaction partners

  1. Studies indicate that mutations in either 3-methylcrotonyl CoA carboxylase (显示 MCCC2 ELISA试剂盒) MCCA (At1g03090) or MCCB (显示 MCCC2 ELISA试剂盒) (At4g34030) block mitochondrial Leu catabolism, as inferred from the increased accumulation of Leu.

Methylcrotonoyl-CoA Carboxylase 1 (Alpha) (MCCC1) 抗原简介

Antigen Summary

This gene encodes the large subunit of 3-methylcrotonyl-CoA carboxylase. This enzyme functions as a heterodimer and catalyzes the carboxylation of 3-methylcrotonyl-CoA to form 3-methylglutaconyl-CoA. Mutations in this gene are associated with 3-Methylcrotonylglycinuria, an autosomal recessive disorder of leucine catabolism.

Gene names and symbols associated with MCCC1

  • methylcrotonoyl-CoA carboxylase 1 (MCCC1) 抗体
  • methylcrotonoyl-CoA carboxylase 1 (Mccc1) 抗体
  • methylcrotonyl-CoA carboxylase alpha chain (MCCA) 抗体
  • methylcrotonoyl-Coenzyme A carboxylase 1 (alpha) (Mccc1) 抗体
  • 1810045E08Rik 抗体
  • 2310058B18Rik 抗体
  • MCC-B 抗体
  • Mcca 抗体
  • MCCalpha 抗体
  • R75106 抗体

Protein level used designations for MCCC1

3-methylcrotonyl-CoA carboxylase 1 , 3-methylcrotonyl-CoA carboxylase biotin-containing subunit , 3-methylcrotonyl-CoA:carbon dioxide ligase subunit alpha , MCCase subunit alpha , methylcrotonoyl-CoA carboxylase subunit alpha, mitochondrial , methylcrotonoyl-Coenzyme A carboxylase 1 (alpha)

56922 Homo sapiens
294972 Rattus norvegicus
838362 Arabidopsis thaliana
72039 Mus musculus
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