ATPaseAssayswith32PATP
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 MgCl25% Norit A activated charcoal in 50 mM NaH2PO4Reaction Mix =___µl motor = 0.5 - 1 µM final concentration (__µl microtubules) 10 µl nucleotide mix = 5 mM Mg·ATP final concentration 30 µl of 100 mM HEPES, pH 7.2 = 10 mM HEPES, pH 7......阅读全文
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
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
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
Agglutination－Assays
Agglutination AssaysREFERENCE: Lanyi, B., and T. Bergan. Methods in Microbiology, Vol 10: 93-168. BACTERIAL AGGLUTINATION: Bacterial agglutination is
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
Cytotoxicity－Assays－Protocol
Cytotoxicity Assays ProtocolCell-mediated cytotoxicity was determined by using a standard microcytotoxicity assay. Briefly, target cells were pelleted
Microtubule－Binding－Assays
MaterialsSiliconized ultracentrifuge microfuge tubesGTP-depleted microtubules6X SDS loading dye1X SDS loading dyeCoomassie Brilliant Blue R 250 (0.8%
Matrigel－invasion－assays
OverviewMatirgel is considered as basement membrane and generated from EHS sarcoma. Matrigel contains not only basement membrane components (collagens
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
cAMP分析－cAMP－Assays
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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
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
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
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
人ATP酶（ATPase）酶联免疫分析
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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
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
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
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/
In－Vitro－prostate－colony－and－sphereforming－assays
1. Prostates were dissected, minced into small pieces with a steel blade, and digested with 0.8 mg/ml collagenase in 10 ml of primary cell medium/
细胞质膜H+ATPase抗体在植物研究的多种应用
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Nature：RAS突变通过VATPase定位到质膜，以激活大胞饮
RAS突变可以说是最难搞定的致癌突变之一了，发现最早，分布最广，虽说有了靶向药，但也只对携带RAS突变的肺癌有较好的效果。几乎全部携带KRAS突变的胰导管腺癌，也成为了当之无愧的癌中之王。 除了自己没法被搞定，RAS突变还会赋予癌细胞一个外挂——大胞饮。这个大胞饮，原本是巨噬细胞用来吃掉那些入
人NaKATP酶(NaKATPase)ELISA试剂盒操作使用说明
我司ELISA试剂盒品质保证，质量优，价格实惠，是您生物实验的首选，如有需要可与我司销售人员联系。本试剂仅供研究使用目的：本试剂盒用于测定人血清，血浆及相关液体样本中人Na-K-ATP酶(Na-K-ATPase)的活性。实验原理：本试剂盒应用双抗体夹心法测定标本中人Na-K-ATP酶(Na-K-AT
线粒体荧光探针大全：TMRM，Mitotracker，JC1（5）
Monoclonal Antibodies Specific for Proteins in the Oxidative Phosphorylation SystemOxidative phosphorylation (OxPhos) activity occurs in the mitochond
细菌感染触发VATPase复合物招募ATG16L1，进而介导细菌自噬
2019年7月18日，北京生命科学研究所邵峰课题组在Cell发表了题为A Bacterial Effector Reveals the V-ATPase-ATG16L1Axis that Initiates Xenophagy的研究文章，通过研究沙门氏菌III型分泌系统效应蛋白SopF，揭示了细
实验室自动化与筛选协会2013亚洲会展短期培训课程简介
短期培训课程I ：生物制剂研发中的高通量筛选 Junma Zhou，博士，上海药明康德新药开发有限公司 刘洁颖博士，上海药明康德新药开发有限公司 In Scope of Short Course - Overview of high-throughput techniques in
与结直肠癌相关的PSMD4基因编码功能描述
26S蛋白酶体是一种多催化蛋白酶复合物，由2个复合物、一个20S核和一个19S调节器组成，具有高度有序的结构。20S核由4个28个不相同亚单位的环组成，2个环由7个α亚单位组成，2个环由7个β亚单位组成。19S调节器由一个碱基（包含6个ATPase亚单位和2个非ATPase亚单位）和一个LID（包含