Alkaline Phosphatases

General description This high-activity recombinant alkaline phosphatase has a minimum Specific Activity of &#8805: 15,000 U/mg (measured at 37 °C), and a minimum purity of &#8805: 95% by HPLC. No animal-derived components are used in the

ALKALINE PHOSPHATASE RED MICROWELL SUBSTRATE COMPONENT A

ALKALINE PHOSPHATASE RED MICROWELL SUBSTRATE COMPONENT B

Steptavidin, a bacterial protein isolated from Streptomyces avidinii, is similar to egg-white avidin in its ability to bind biotin, and has been used as a replacement for egg-white avidin because of its more favorable chemical properties. Conjugates

General description The product is ready to use buffered alkaline phosphatase substrate consist of p -nitrophenylphosphate (pNPP). This is the advanced substrate system contains insoluble stabilizer that enhances the stability and reactivity as

1,000 U Conjugation Grade Ammonium Sulfate Suspension Source: Calf Intestine Adenosine Deaminase: &lt=0.001% Concentration (37 C): &gt7500U/ml Phosphodiesterase: &lt=0.

1,000 U Conjugation Grade Ammonium Sulfate Suspension Source: Calf Intestine Adenosine Deaminase: &lt=0.001% Concentration (37 C): &gt7500U/ml Phosphodiesterase: &lt=0.

General description &#945:-D-Glucose 1,6-bisphosphate was found to be at a concentration of between 10 &#956:m and 600 &#956:m in various tissues including liver, brain and kidney. Application &#945:-D-Glucose 1,6-bisphosphate is used in the

General description The previously assigned protein identifier A4D1D4 has been merged into P21439. Full details can be found on the UniProt database.

Specificity Alkaline phosphatase (AP). MAB1012 has a high affinity and recognizes an AP determinant resistant to denaturation by SDS-PAGE.

General description Recombinant DNA technology enables the insertion of specific short sequences into genes of interest. This can provide an ′affinity handles′ (tags) for the selective identification and purification of the recombinant p

General description Recombinant DNA technology enables the insertion of specific short sequences into genes of interest. This can provide an ′affinity handles′ (tags) for the selective identification and purification of the recombinant p