14-497 Sigma-AldrichPKC η Protein, active, 10 µg
Active, N-terminal His6-tagged, recombinant amino acids 2-end, of human PKC eta. For use in Kinase Assays.
More>> Active, N-terminal His6-tagged, recombinant amino acids 2-end, of human PKC eta. For use in Kinase Assays. Less<<Recommended Products
Overview
Replacement Information |
---|
References |
---|
Product Information | |
---|---|
Quality Level | MQ100 |
Applications | |
---|---|
Application | Active, N-terminal His6-tagged, recombinant amino acids 2-end, of human PKC eta. For use in Kinase Assays. |
Key Applications |
|
Physicochemical Information |
---|
Dimensions |
---|
Materials Information |
---|
Toxicological Information |
---|
Safety Information according to GHS |
---|
Safety Information |
---|
Storage and Shipping Information | |
---|---|
Storage Conditions | 6 months at -70°C |
Packaging Information | |
---|---|
Material Size | 10 µg |
Material Package | Also available in 250 µg size --call for pricing and availability and reference catalog number 14-497M when ordering the 250 µg size. |
Transport Information |
---|
Supplemental Information |
---|
Specifications |
---|
Global Trade Item Number | |
---|---|
Catalogue Number | GTIN |
14-497 | 04053252674617 |
Documentation
PKC η Protein, active, 10 µg SDS
Title |
---|
PKC η Protein, active, 10 µg Certificates of Analysis
Title | Lot Number |
---|---|
PKC eta, active - 25609U-B | 25609U-B |
FAQ
Question | Answer |
---|---|
Why is it important to shake the reaction mixture during the incubations? | It is important to shake the reaction mixture during incubations so that the substrate and the enzyme get good interaction. If you do not have access to a shaking incubator, use a water bath for the incubations, removing the tubes regularly to vortex. |
What type of buffer is best for lysis when attempting to preserve a protein? | The best buffer is Buffer A. It is composed of 50mM Tris/HCl, pH 7.5, 1mM EGTA, 1mM EDTA, 1mM Sodium Orthovanadate (activated), 10mM Na B-glycerolphosphate, 50mM NaF, 5mM Na pyrophosphate, 1% w/v Triton X-100, 0.1% w/v 2-mercaptoethanol, 1ug/ml each of aprotinin, leupeptin and pepstatin, 1mM PMSF and 1mM microcystin (this is optional). QS with water. You may store Buffer A in aliquots at -20°C for 6 months. |
What is the Molar extinction coefficient for Adenosine 5'-[g32P]triphosphate ([g32P]ATP) used in the kinase assay? | The Molar extinction coefficient is 15400. |
What is the best way to store and thaw enzymes? | In order to maintain activity of enzymes, we recommend a slow thaw and aliquot storage. To do this, remove the full vial from the freezer and place under cold running tap water. Once thawed, place the vial on ice, gently mix, than make aliquots. Using liquid nitrogen or an ethanol/dry ice bath, flash freeze the aliquots. Store aliquots at the recommended temperature. |
When using p81 paper (phosphocellulose squares), what is the purpose of the acetone wash? | The purpose of washing the p81 squares in acetone is mostly to help them dry faster, but it also can help to eliminate low specificity binding. |
Some of my enzyme preparations require Brij-35, what is its purpose? | The role of Brij-35 is to function as a mild detergent, which prevents aggregation in active kinases. |