نتایج جستجو برای: lactate dehydrogenase assay

تعداد نتایج: 307059  

Journal: :Clinical chemistry 1976
D McKenzie P I Clark A R Henderson

We offer an assessment of the accuracy of the thin-layer agarose fluorescent technique of Elevitch et al. [Am. J. Clin. Pathol. 46, 692 (1966)]. We used semi-purified human lactate dehydrogenase isoenzymes 1 and 5. Both the lactate lead to pyruvate and pyruvate lead to lactate assays [Clin. Chem. 20, 1462 (1974)] appear to give, within the errors of the techniques used, a substantially unbiased...

Journal: :Clinical chemistry 1977
S N Buhl K Y Jackson R Lubinski R E Vanderlinde

Optimal reaction conditions to sassay human lactate dehydrogenase (lactate-to-pyruvate) were established for isoenzymes 1 and 5 at 25, 30, and 37 degrees C in diethanolamine and 2-amino-2-methyl-1,3-propanediol. Different substrate concentrations are required at each temperature. The conditions permit measurement of lactate dehydrogenase 1 and 5 with the lowest substrate concentrations that all...

Journal: :iranian journal of nursing and midwifery research 0
zahra maghsoudi afshin shiranian gholamreza askai reza ghaisvand

abstract background: athletes’ recovery is important in improving their performance. nutritional strategies can be effective in enhancing recovery rate. choosing the best food items in appropriate intervals can play effective roles in resynthesis of fuels and recovery of muscle injury. beverage micro and macronutrient content are helpful in fuel restoration. in this study, we assess the effects...

2001
Takahisa Ohta

The gene encoding D-lactate dehydrogenase (D-lactate: NAD+ oxidoreductase, EC 1.1.1.28) of Lactobacillus plantarum has been sequenced, and expressed in Escherichia coli cells with an inducible expression plasmid, in which the 5‘-noncoding region of the gene was replaced with the tac promoter. Comparison of the sequence of D-laCtate dehydrogenase with L-lactate dehydrogenases, including the L. p...

Journal: :iranian journal of parasitology 0
daniel getacher feleke department of medical parasitology and mycology, school of public health, international campus, tehran university of medical sciences, tehran, iran mehdi nateghpour department of medical parasitology and mycology, school of public health, international campus, tehran university of medical sciences, tehran, iran and center for research of endemic parasites of iran, tehran university of medical sciences, tehran, iran afsaneh motevalli haghi department of medical parasitology and mycology, school of public health, international campus, tehran university of medical sciences, tehran, iran homa hajjaran department of medical parasitology and mycology, school of public health, international campus, tehran university of medical sciences, tehran, iran leila farivar department of medical parasitology and mycology, school of public health, international campus, tehran university of medical sciences, tehran, iran mehdi mohebali department of medical parasitology and mycology, school of public health, international campus, tehran university of medical sciences, tehran, iran

background: parasite lactate dehydrogenase ( p ldh) is extensively employed as malaria rapid diagnostic tests (rdts). moreover, it is a well-known drug target candidate. however, the genetic diversity of this gene might influence perfor­mance of rdt kits and its drug target candidacy. this study aimed to determine polymorphism of p ldh gene from iranian isolates of p. vivax and p. falciparum. m...

2006
Victoria R. Polonis Garth R. Anderson John Brzykcy Adrian O. Vladutiu Kenneth F. Manly

An unusual isozyme of lactate dehydrogenase, láclate dehydrogenase associated with Kirsten murine sarcoma virus (LDHk) was found in the sera of many patients with malignant tumors, while the sera of healthy persons had little or no such activity. This isozyme was detectable only when assayed in a nitrogen atmosphere, and its activity showed little or no relationship to the total lactate dehydr...

Journal: :Clinical chemistry 1984
C H McMurray W J Blanchflower D A Rice

This assay for 3-hydroxybutyrate in plasma or serum, based on kinetic initial-rate techniques, has been optimized with respect to initial rate and linearity as follows: pH 8.5, hydroxybutyrate dehydrogenase 62.5 U/L, and NAD+ concentration 20 mmol/L. We have used the assay satisfactorily with both the Gilford 103 and Hitachi 705 discrete analyzers, obtaining results that compare well with those...

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