June 2, 2023

Himediea Coa

Lab Reagents

Himedia Coa Laboratories manufactures the himediea coa reagents distributed by Genprice. The Himediea Coa reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact himedia coa. Other Himediea products are available in stock. Specificity: Himediea Category: Coa

Biology information

Acyl-CoA synthetase, recombinant
NATE-1682 1ku
EUR 712.8

Ac-CoA Synthase Inhibitor1
HY-104032 5mg
EUR 176.4

anti-Acetoacetyl CoA synthetase
YF-PA20683 50 ul
EUR 435.6
Description: Mouse polyclonal to Acetoacetyl CoA synthetase

anti-Acetoacetyl CoA synthetase
YF-PA20684 50 ug
EUR 435.6
Description: Mouse polyclonal to Acetoacetyl CoA synthetase

anti-Acetoacetyl CoA synthetase
YF-PA20685 100 ug
EUR 483.6
Description: Rabbit polyclonal to Acetoacetyl CoA synthetase

anti-Acetyl CoA synthetase
YF-PA19911 50 ug
EUR 435.6
Description: Mouse polyclonal to Acetyl CoA synthetase

HMG-CoA Reductase Antibody
3952-100 each
EUR 424.8

HMG-CoA Reductase Antibody
3952-30T each
EUR 175.2

HMG-CoA Blocking Peptide
3952BP-50 each
EUR 183.6

Recombinant Human Acetyl-COA Acyltransferase
7-02362 5µg Ask for price

Recombinant Human Acetyl-COA Acyltransferase
7-02363 20µg Ask for price

Recombinant Human Acetyl-COA Acyltransferase
7-02364 1mg Ask for price

PicoProbe Acetyl-CoA Assay Kit
55R-1369 100 assays
EUR 967.2
Description: Assay Kit for detection of Acetyl-CoA in the research laboratory

Recombinant Human Methylmalonyl CoA Epimerase
7-02737 5µg Ask for price

Recombinant Human Methylmalonyl CoA Epimerase
7-02738 20µg Ask for price

Recombinant Human Methylmalonyl CoA Epimerase
7-02739 1mg Ask for price

Methylmalonyl-CoA epimerase Recombinant Protein
92-387 0.05 mg
EUR 437.1
Description: Methylmalonyl-CoA epimerase, mitochondrial（MCEE）is an enzyme which belongs to the glyoxalase I family. It converts (S)-methylmalonyl-CoA to the (R) form, catalyses the following chemical reaction: (R)-methylmalonyl-CoA (S)-methylmalonyl-CoA. It plays an important role in the catabolism of fatty acids with odd-length carbon chains. This protein deficiency is an autosomal recessive inborn error of AA metabolism, involving valine, threonine, isoleucine and methionine. This organic aciduria can appear in the neonatal period with life-threatening metabolic acidosis, hyperammonemia, feeding difficulties, pancytopenia and coma.