NuclearRunOnTranscriptionAssays

Nuclear “run-on” (or “run-off”) transcription assays have been used to obtain quantitative information about the relative rates of transcription of different genes in nuclei isolated from a particular tissue or organ. This information can then be used in analyzing the factors that control the expression of specific genes. These assays are complimentary to measurements of the levels of mRNA species present i......阅读全文

Nuclear-RunOn-Transcription-Assays

Nuclear “run-on” (or “run-off”) transcription assays have been used to obtain quantitative information about the relative rates of transcription o

Reverse-Transcription-of-RNA

实验概要The purpose of Reverse transcription of RNA is acquiring cDNA for follow research.实验原理Reverse  Transcription (RT reaction) is a process in which s

REVERSE-TRANSCRIPTION-PCR:

REVERSE TRANSCRIPTION PCR:RNA -> LOTS OF DNAContentsReverse Transcription ReactionPolymerase Chain ReactionReverse Transcription Reaction:This provide

Cellulase-assays

Cellulase enzymes show activity during the ripening of some fruits, where their effects on cell walls results in softening of the fruit. In cases of p

Carbohydrate-Assays

Carbohydrate AssaysREFERENCE: Wright and Rebers, Anal. Biochem. 49: 307-319, 1972.OBJECTIVE: To determine the relative amounts ofLPS carbohydrates pre

Agglutination-Assays

Agglutination AssaysREFERENCE: Lanyi, B., and T. Bergan. Methods in Microbiology, Vol 10: 93-168. BACTERIAL AGGLUTINATION: Bacterial agglutination is

Cellulase-assays

实验概要        Cellulase enzymes show activity during the ripening of some fruits, where their effects on cell walls results in softening of the frui

RNA-polymerase-III-transcription

Unlike the RNA polymerase II that transcribes a large variety of genes that encode proteins, RNA polymerase III transcribes only a limited number of g

Matrigel-invasion-assays

OverviewMatirgel is considered as basement membrane and generated from EHS sarcoma. Matrigel contains not only basement membrane components (collagens

Microtubule-Binding-Assays

MaterialsSiliconized ultracentrifuge microfuge tubesGTP-depleted microtubules6X SDS loading dye1X SDS loading dyeCoomassie Brilliant Blue R 250 (0.8%

Cytotoxicity-Assays-Protocol

Cytotoxicity Assays ProtocolCell-mediated cytotoxicity was determined by using a standard microcytotoxicity assay. Briefly, target cells were pelleted

DNA-Fragmentation-Assays-for-Apoptosis

Protocol I: Triton X-100 Lysis BufferIn 96 flat-wells plate, incubate 4x10 6 target cells (40 wells of 105 per well) with desired concentration of eff

Coimmunoprecipitation-assays

co-IP assays can be performed between endogenous proteins or transiently or stably expressed exogenous - usually tagged - proteins. The advantage to u

SAPK/Jun-kinase-assays

Preparation of cell lysate:1. For cells in suspension, grow in DMEM with 10% FCS and then the day before you do the experiment spin the cells down (1

PLAQUE-ASSAYS-FOR-ADENOVIRUS-TITRATION

-Set up 60 mm dishes of P11 cells to be 100 confluent at time of infection. -Remove medium from dishes, add 0.2 to 0.5 ml virus and adsorb for 30 – 60

cAMP分析-cAMP-Assays

cAMP AssaysGouzel Karimova and Daniel LadantUnite Postulante de Biochimie des Interactions Macromoleculaires, Departement de Biologie Structurale et C

Transcription-factor-CREB-and-its-extracellular-signals

The transcription factor CREB binds the cyclic AMP response element (CRE) and activates transcription in response to a variety of extracellular signal

NFAT-and-Hypertrophy-of-the-heart-(Transcription-in-the-broken-heart)

Hypertrophy associated with both hypertension and obstruction to ventricular outflow leads to pathologic cardiac growth and it is associated with incr

Transcription-Regulation-by-Methyltransferase-of-CARM1

Several forms of post-translational modification regulate protein activities. Recently, protein methylation by CARM1 (coactivator-associated arginine

Microtubule-(MT)/Organelle-Motility-Assays

Rapidly thaw and immediately place on ice one aliquot each of axonemes, Golgi or ER membranes, 45 uM tubulin, rat liver cytosol, and 20x energy regene

Fragment-Complementation-and-Coimmunoprecipitation-Assays-for-...

Plant disease resistance (R) proteins confer protection against specific pathogens or pathogen isolates. R proteins function by recognizing pathog

Preparation-of-Luciferin-for-In-Vitro-and-In-Vivo-Bioluminescent-Assays

Preparation of Luciferin forIn Vitro Bioluminescent AssaysMaterials• D-Luciferin Firefly, potassium salt, 1.0 g /vial(Caliper Life Sciences Part Numbe

Preparation-of-Luciferin-for-In-Vitro-and-In-Vivo-Bioluminescent-Assays

实验概要Reagent  for immunoassay, ligand binding assay and ligand receptor assay in  which luciferin is covalently bonded to a molecule having biological

ATPase-Assays-with-32PATP

MaterialsPurified Motor Protein, 20-80 µMNucleotide Mix =50 mM Mg·ATP gamma-32P-ATP to give 5 000 - 10 000 cpm/nmol 10 mM HEPES, pH 7.2 1 mM EGTA 1 mM

Preparation-of-Luciferin-for-In-Vitro-and-In-Vivo-Bioluminescent-Assays

实验概要Reagent  for immunoassay, ligand binding assay and ligand receptor assay in  which luciferin is covalently bonded to a molecule having biological

Isolation-and-Transcription-Profiling-of-Purified-Uncultured-Human-Strom...

Isolation and Transcription Profiling of Purified Uncultured Human Stromal Stem CellsIsolation and Transcription Profiling of Purified Uncultured Huma

Multistep-Regulation-of-Transcription-by-Pitx2

Many transcription factors play essential roles in normal development by determining the proliferation and differentiation of cells. The coordinated t

Steady-State-ATPase-Assays-Coupled-Enzyme-System

MaterialsTubulin (>5 mg/mL)100 mM Mg·GTP4 mM Taxol in DMSOPM =100 mM PIPES pH 6.82 mM EGTA1 mM Mg2SO4Motor protein (>95% purity; 15-20 µM)Cuvettes (20

Flow-Cell-Assays-with-Microtubules:-Motility/Dynamics-in-Fluorescence

Flow cell assays are very useful for studying microtubule motility, microtubule dynamics, kinetochore-microtubule interactions and action of severing/

Transcription,-Translation-of-S35Radiolabelled-Protein-and-Binding-to-GST

Prepare the template by linearizing 25ug plasmid DNA at the 3'' end of the insert. Phenol / chloroform extract, ethanol / NaCl precipitate and