027-59234612(+86)
EIAab
Home  >  ELISA Kit  >  Rat Acadvl ELISA Kit
Acadvl (GeneName), Very long-chain specific acyl-CoA dehydrogenase, mitochondrial (ProteinName), ACADV_RAT.
Product Name:

Rat Acadvl/ Very long-chain specific acyl-CoA dehydrogenase, mitochondrial ELISA Kit

Cat.#:
-
Brand:
EIAab®
Regulatory Status:
Alternative:

VLCAD, Vlcad

Detection Method:
ELISA
Specificity:
Natural and recombinant rat Very long-chain specific acyl-CoA dehydrogenase, mitochondrial
Sample Type:
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Sample Data:
Research Area:
Cardiovascular
Rat Acadvl ELISA Kit
Size & Price: Sign In.
×
Rat Acadvl ELISA Kit
Email *
Message *
Please Sign In.
Product Datasheets


General Annotation


Sub Unit:
Homodimer.


Function:
Active toward esters of long-chain and very long chain fatty acids such as palmitoyl-CoA, mysritoyl-CoA and stearoyl-CoA. Can accommodate substrate acyl chain lengths as long as 24 carbons, but shows little activity for substrates of less than 12 carbons.


Subcellular Location:
Mitochondrion inner membrane


This product has not yet been referenced specifically in any publications.

[1].
"Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency."

[2].
"Molecular heterogeneity in very-long-chain acyl-CoA dehydrogenase deficiency causing pediatric cardiomyopathy and sudden death."

[3].
"Very long chain acyl-coenzyme A dehydrogenase deficiency with adult onset."

[4].
"Assignment of the human mitochondrial very-long-chain acyl-CoA dehydrogenase gene (LCACD) to 17p13 by in situ hybridization."

[5].
"Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene."

[6].
"Mutation analysis of very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency: identification and characterization of mutant VLCAD cDNAs from four patients."

[7].
"Cloning of human very-long-chain acyl-coenzyme A dehydrogenase and molecular characterization of its deficiency in two patients."

[8].
"Purification of human very-long-chain acyl-coenzyme A dehydrogenase and characterization of its deficiency in seven patients."

[9].
"Genomic DNA organization of human mitochondrial very-long-chain acyl-CoA dehydrogenase and mutation analysis."

[10].
"Dysregulation of very long chain acyl-CoA dehydrogenase coupled with lipid peroxidation."
Close
Sample Data
Close
Sample Data
Close
Sample Data
My Cart close
Attention close
History close
Clear All
Comparison close
User
My Cart
Attention
History
Comparison
Top
Message
close_message
Product Name *
Email *
Message: *
Inform
new Message
Size Quantity Price ($) Subtotal 1 ($)
Subtotal 2: $
triangle
Size Quantity Price ($)
Do you want to be our agent and get a lower discount?
Please contact us:
Tel:027-59234612(+86)
Fax:027-59759960(+86)
Email:sales@eiaab.com