DGKAssay

Buffers:- 2X buffer10 ml 0.5 M imidazol, pH 6.60.21 g LiCl1.25 ml 1 M MgCl21.0 ml 0.1 M EGTA, pH 6.6--> Bring volume up to 50 ml with distilled water.- dilution buffer1 ml 0.5 M imidazol, pH 6.62.5 ml 20 mM diethylenetriaminepentaacetic acid (DTPA)--> Bring volume up to 50 ml with distilled water.Reaction Mixture:solution [stock] vol/tube # samples total vol.2X buffer - 50 µl X _______ = _______DTT 1 M 0.2 µl X......阅读全文

In-Vitro-Protein-Ubiquitination-Assay

Ubiquitination is one of the most important posttranslational modifications in all eukaryote organisms. Ubiquitin-activating enzyme (E1), ubiquiti

Cell-Clonogenic-Survival-Assay

DescriptionAllows one to test the capability of adherent cells to survive and replicate following insult with chemicals or radiation. Procedure1. Grow

Cr-Release-Cytotoxicity-assay

DescriptionCytotoxic activities of mNK cells are examined in 51Cr release assay from target cells ProcedureEffector cells (mNK cells) are seeded into

DNA-laddering-assay-for-treated-cells

Characteristics of this procedure: I found the procedure described by Gong et al. to be a convenient and successful method to detect DNA ladderin

The-UnderAgarose-Migration-Assay

overviewThe Under-Agarose assay is a useful method for observing the response of a cell population to one or more chemoattractant sources. The behavio

XC-Assay-of-MoMLV-Virus-Stocks

MaterialsWildtype MoMLV virus aliquot.  Stored at -80ºC.Medium:  DMEM + 10% FBSNIH 3T3 TK- cellsXC cellsPolybrene 1000x stock = 4 mg/mL, sterile filte

SOFT-AGAR-ASSAY-FOR-COLONY-FORMATION

Note: All volumes are calculated to cater for four plates per point.Base Agar1. Melt 1% Agar (DNA grade) in microwave, cool to 40 in a waterbath. War

Chick-Chorioallantoic-Membrane-(CAM)-Assay

CAM ASSAYShell-less embryo cultureFertilized white leghorn chicken eggs (SPAFAS Inc., Norwich, CT) were received at day 0 andincubated for 3 days at 3

Apoptosis-TUNEL-assay-(Paraffin-Sections)

Protocol for Paraffin Sections:Dewax paraffin sections:Incubate slides, 55°C, 30 min.Xylenes, 2 times, 2 min. each100% EtOH, 2 times, 2 min. each95% E

alamarBlue®-Cell-Viability-Assay-Protocol

实验概要Cell health can be  monitored by numerous methods. Plasma membrane integrity, DNA  synthesis, DNA content, enzyme activity, presence of ATP, and c

Chemotaxis-Assay趋化性实验

Springer Lab,The CBR Institute for Biomedical Research, Inc. Department of Pathology Harvard Medical Schoolhttp://cbr.med.harvard.edu/investigators/sp

NKcell-cytotoxicity-assay

Outline:To measure NK cell killing, suitable target cells are labeled with 51Cr, washed and incubated together with the killer cells (and treatments).

Invitro-Phagocytosis-Assay-of-Macrophages

IntroductionThe term phagocytosis itself describes its mean phage = engulfment; cytosis: cell process. In other words, phagocytosis is the cellular pr

Apoptosis-TUNEL-Assay-(frozen-sections)

Protocol for Frozen Sections:Warm 150ml 4% Paraformaldehyde/1x PBS to RT. Fix slides in it, 20 min., RT.1x PBS rinse, 2 times.1x PBS, 30 min., RT. Beg

NB2cell-proliferation-assay

before start: thaw cells from liquid nitrogen, grow in 75cc flask (T75) in Fischer's medium MM (maintenance medium) until content gets cloudy and st

Assay-of-Tyrosine-Kinases-Using-Synthetic-Peptides

实验概要         Small synthetic peptide substrates are especially well suited for applications such as assays of tyrosine kinases in permeabilized

James-Hardwicks-angiotensin-assay-protocol

 This specific procedure was developed to assay the activity of the Lck kinase expressed from a retroviral vector in rat fibroblasts. You can obv

Assay-of-superoxide-dismutase-activity1

Assay of superoxide dismutase activity by combining electrophoresis and densitometryAbstract. A modified technique was developed to assay superoxide d

Assay-of-superoxide-dismutase-activity3

Botanical Bulletin of Academia Sinica, Vol. 37, 1996The method using NBT as a superoxide radical competitor and a color indicator was also explored to

Assay-of-superoxide-dismutase-activity2

Cuvette holders in the sample chamber of the spectrophotometer were thermo-controlled at 25°C. For the blank test, 100 ml of 50 mM potassium phosphate

MINICHROMOSOME-MICROTUBULE-BINDING-ASSAY2

HYBRIDIZATION.Prehybridize blot at 65oC for ~3h in Church buffer containing 0.5mg/ml denature salmon sperm DNA (usually 14ml Church buffer plus 0.7ml

IFNy-Elispot-Assay...

实验概要The  Elispot (Enzyme Linked Immuno-Spot) assay provides an effective method  of measuring the antibody or cytokine production of immune cells on t

Endothelial-wound-healing-(cell-migration)-assay

DescriptionThis is a simple assay that can be used in any cell culture lab setup to test the effect of different compounds on endothelial cell migrati

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

荧光素酶检测(Luciferase-assay)

Introduction Luciferase can be used as a reporter gene to measure the activity of promoters, and/or the transfection efficiency. Aims You will be prov

与白血病相关的DGKH基因编码功能描述

该基因编码二酰甘油激酶(DGK)酶家族的一个成员。这个家族的成员参与调节二酰甘油和磷脂酸的细胞内浓度。这种基因的变异与双相情感障碍有关。另外,还发现了剪接转录变体。This gene encodes a member of the diacylglycerol kinase (DGK) enzyme

DGKH基因突变与药物因子介绍

该基因编码二酰甘油激酶(DGK)酶家族的一个成员。这个家族的成员参与调节二酰甘油和磷脂酸的细胞内浓度。这种基因的变异与双相情感障碍有关。另外,还发现了剪接转录变体。This gene encodes a member of the diacylglycerol kinase (DGK) enzyme

DGKH基因编码功能及结构描述

该基因编码二酰甘油激酶(DGK)酶家族的一个成员。这个家族的成员参与调节二酰甘油和磷脂酸的细胞内浓度。这种基因的变异与双相情感障碍有关。另外,还发现了剪接转录变体。This gene encodes a member of the diacylglycerol kinase (DGK) enzyme

Use-of-the-Bradford-Protein-Assay-in-a-Microtiter-Plate-Format

Introduction  The Bradford protein assay is a simple procedure for determination of protein concentrations in solutions that depends upon the change

Critical-Appraisal-of-the-MTT-Assay-in-the-Presence-of-Rottlerin-1

Rottlerin is a natural product isolated from Mallotus philippinensis. This polyphenolic compound, originally described as a selective inhibitor of PK