新技术:InCellWesternAssay2

III. Experimental ConsiderationsProper selection of microplates can significantly affect the results of your analysis, as each plate has its own characteristics including well depth, plate autofluorescence, and well-to-well signal crossover. Use the general considerations for microplate selection provided below.In-Cell Western analyses use detection at the well surface with no liquid present. This results in minimal ......阅读全文

新技术:InCell-Western-Assay

In-Cell Western AssayComplete Sample Protocol Detailing the SeedingStimulation, and Detection of the HeLa CellularResponse to Epidermal Growth FactorI

新技术:InCell-Western-Assay2

III. Experimental ConsiderationsProper selection of microplates can significantly affect the results of your analysis, as each plate has its own chara

Pectinase-assay

Pectinases are actually a mixture of enzymes, which, along with others such as cellulase, are widely used in the fruit juice industry where they are

Protease-assay

In certain fruits, such as pineapples and mangoes, the flesh contains protein-digesting enzymes (proteases). These may play a part in helping to soft

Protease-assay

实验概要         In certain fruits, such as pineapples and mangoes, the flesh contains protein-digesting enzymes (proteases). These may play a part

DGK-Assay

Buffers: - 2X buffer 10 ml 0.5 M imidazol, pH 6.6 0.21 g LiCl 1.25 ml 1 M MgCl2 1.0 ml 0.1 M EGTA, pH 6.6 --> Bring volume up to 50 ml with distille

Phosphate-Assay

1. Make standards using sodium phosphate at the following uM concentrations: 0, 2, 5, 7, 10, 20, 40, 60, and 80. Use the screw top glass tubes.2. Dry

TUNEL-assay

PROTOCOL:•Deparaffinize and rehydrate slides:3 x 3´ Xylene3 x 2´ 100% ethanol1 x 2´ 95%, 80%, 70% ethanol (each)1 x 5´ 1x PBS•Microwave antigen retrie

Polygalacturonase-assay

This enzyme is famous for being involved in the development of the GMO tomatoes (more information from the link at the foot of this page). The cells o

Aspartate-Assay

实验概要The  Aspartate Assay Kit provides a simple, convenient assay to measure  aspartate in a variety of samples. In the assay, aspartate is converted  

Motility-Assay

DescriptionVarious phenotypic characteristics are requiredfor a cancer cell to successfully complete the metastaticcascade. Among these, acquisition o

Bradford-Assay

The bradford dye-binding assay is a colorimetric assay for measuring total protein concentration. It involves the binding of Coomassie Brilliant blue

MTT-Assay

 This procedure is for cells in 96 well plates, if larger plates are used then adjust volumes accordingly.1 Make a solution of 5mg/ml MTT dissolved in

Bradford-Assay

Bradford AssayThe bradford dye-binding assay is a colorimetric assay for measuring total protein concentration. It involves the binding of Coomassie B

Chemotaxis-Assay

PurposeThe purpose of a chemotaxis assay is to determine whether your protein or small molecule of interest has chemotactic activity on a specific cel

Assay-of-Phospholipase-A-Activity

Phospholipases of the A type constitute a large family of esterases that catalyze the hydrolysis of the fatty acid ester bonds in phospholipids a

Actin-Capture-Assay

David Amberg Dialyze purified GST fusion proteins and actin into PBS + 1mM MgCl2 . Mix 5ug actin into 50ul total volume binding buffer. Mix

Needle-Assay-for-Chemotaxis

Devreotes Lab, John Hopkins Medical Institutions http://www.hopkinsmedicine.org/cellbio/devreotes/needle.htm Equipment and chemicals Zeiss

Assay-for-the-Micrococcal-Nuclease

Method: Essentially that described by Heins et al. (1966) based upon the release of acid soluble oligonucleotides following nuclease digestion of DNA

BIURET-PROTEIN-ASSAY

BIURET PROTEIN ASSAY MATERIALS Biuret Reagent Bovine serum albumin (BSA) Spectrophotometer and tubes PROCEDURE Prepare standard d

In-vitro-Sphingomyelinase-Assay

Reagents: Lysis buffer 25 mM Tris-HCl, pH 7.4 5 mM EDTA 1 mM ATP 20 µg/ml CLAP 1 mM PMSF Buffer A 10 mM MgCl2 0.2 M Tris-HCl, pH 7.4 0.2 % Triton X

ELISA-Inhibition-Assay

ELISA Inhibition AssaySensitize a 96-well microtiter plate with purified antigen.Prepare a solution of the purified antigen of interest in phosphate b

cell-proliferation-assay

cell proliferation assaybefore start:thaw cells from liquid nitrogen, grow in 75cc flask (T75) in Fischer's medium MM (maintenance medium) until c

Leaf-GUS-Assay

一、实验试剂 GUS Buffer (500 ml) 2.0478 g   Na2HPO4 1.2688 g   NaH2PO4 (=50 mM NaPi pH7.0) 10 ml    0.5 M EDTA (=10 mM) 0.5 g    Triton X-100 0.5 g     N-L

HISTONE-KINASE-ASSAY

PROTOCOLTo 1.5 mL eppendorf tubes add:200 µg of protein extract (see Western blot protocol for protein sample preps)q.s. to 300 µL with RIPA (with pro

Pheromone-Halo-Assay

-Use sterile technique and sterile solutions throughout this method.-1. Grow a starter culture at 30 C with shaking (250 rpm) until it reaches saturat

Glucosamine-Rapid-Assay

Glucosamine Rapid AssayMRTHOD:Place sample (containing 0.5 - 10 µg GlcN) in a Pyrex screw capped tube.Add HCl to a final concentration of 2N and a fin

Leaf-GUS-Assay

实验概要a protocol for Leaf GUS Assay This protocol is for small samples (usually single leaf from 21DAI plants), scale up for larger samplesAs there are

Tube-formation-assay

DescriptionThis is a fast and easy assay to test the angiogenic/anti-angiogenic properties of molecules. As compared to other angiogenesis assays, suc

Bradford-protein-assay

Bradford protein assayConsiderations for useThe Bradford assay is very fast and uses about the same amount of protein as the Lowry assay. It is fairly