027-59234612(+86)
EIAab
Home  >  ELISA Kit  >  Rat Acads ELISA Kit
Acads (GeneName), Short-chain specific acyl-CoA dehydrogenase, mitochondrial (ProteinName), ACADS_RAT.
Product Name:

Rat Acads/ Short-chain specific acyl-CoA dehydrogenase, mitochondrial ELISA Kit

Cat.#:

E10434r

Brand:
EIAab®
Regulatory Status:
Alternative:

SCAD, Butyryl-CoA dehydrogenase

Detection Method:
ELISA
Specificity:
Natural and recombinant rat Short-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 Acads ELISA Kit
Size & Price: Sign In.
×
Rat Acads ELISA Kit
Email *
Message *
Please Sign In.
Product Datasheets


General Annotation


Sub Unit:
Homotetramer.


Function:
Introduces a double bond at position 2 in saturated acyl-CoAs of short chain length, i.e. less than 6 carbon atoms.


Subcellular Location:
Mitochondrion matrix


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

[1].
"The 625G>A SCAD gene variant is common but not associated with increased C4-carnitine in newborn blood spots."

[2].
"The frequency of short-chain acyl-CoA dehydrogenase gene variants in the US population and correlation with the C(4)-acylcarnitine concentration in newborn blood spots."

[3].
"Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiency."

[4].
"Identification of four new mutations in the short-chain acyl-CoA dehydrogenase (SCAD) gene in two patients: one of the variant alleles, 511C-->T, is present at an unexpectedly high frequency in the general population, as was the case for 625G-->A, together conferring susceptibility to ethylmalonic aciduria."

[5].
"Structural organization of the human short-chain acyl-CoA dehydrogenase gene."

[6].
"Identification of two variant short chain acyl-coenzyme A dehydrogenase alleles, each containing a different point mutation in a patient with short chain acyl-coenzyme A dehydrogenase deficiency."

[7].
"Molecular cloning and nucleotide sequence of complementary DNAs encoding human short chain acyl-coenzyme A dehydrogenase and the study of the molecular basis of human short chain acyl-coenzyme A dehydrogenase deficiency."

[8].
"The minor C-allele of rs2014355 in ACADS is associated with reduced insulin release following an oral glucose load."

[9].
"A genome-wide perspective of genetic variation in human metabolism."

[10].
"Misfolding of short-chain acyl-CoA dehydrogenase leads to mitochondrial fission and oxidative stress."
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