1. INJ Inject-A-Lume h-Coelenterazine 注射型h-腔肠素
【产品货号】Cat#301、CAS#50909-86-9
【产品规格】1kit、10kits
【产品简介】注射型h-腔肠素,纯度高(99%),针对活体研究进行优化。苯甲基腔肠素(h-CTZ)封装于小体积的无菌注射瓶中。每个试剂盒提供两瓶500 µg的注射型h-CTZ和一瓶无菌注射型稀释液。仅供动物使用。
【使用案例】
Rd R W, Oner S S, Lanier S M, et al. Direct Coupling of a Seven-Transmembrane-Span Receptor to a Gαi G-Protein Regulatory Motif Complex.[J]. Molecular Pharmacology, 2015, 88.
Ciruela F, Fernández-Dueñas V. GPCR oligomerization analysis by means of BRET and dFRAP.[J]. Methods in Molecular Biology, 2015, 1272(1272):133-41.
Schena A, Griss R, Johnsson K. Modulating protein activity using tethered ligands with mutually exclusive binding sites.[J]. Nature Communications, 2015, 6.
2. Coelenterazine-SOL in vivo 水溶性腔肠素(活体研究)
【产品货号】cat#3031
【产品规格】500µg、1mg、10mg
【产品简介】天然腔肠素被制定为水溶性的(天然腔肠素+无毒水溶性添加剂),可安全应用于海肾萤光素酶的活体成像。腔肠素经常溶于丙二醇(PG)结合其他醇类的混合溶剂中,应用于活体成像研究。短时间内静脉注射大剂量PG是有毒性的,包括高渗性、增加阴离子代谢性酸中毒(由于乳酸性酸中毒)、急性肾损伤以及血性症候群。使用水溶性腔肠素可避免上述问题,它被制定为等渗压以及易于被肾脏分泌的,从而避免重复性的活体注射。水溶性的腔肠素最高注射浓度可达500 µg/100 µl,在机体内能够达到一个相当高腔肠素水平,带来强烈的海肾荧光素信号。
【使用案例】
Yao M, Lu X, Lei Y, et al. Conditional Inducible Triple-Transgenic Mouse Model for Rapid Real-Time Detection of HCV NS3/4A Protease Activity.[J]. Plos One, 2016, 11(3).
3. Coelenterazin h 腔肠素h
【产品货号】cat#301 、CAS#50909-86-9
【产品规格】500µg、1mg、5mg、10mg
【产品简介】腔肠素h,是一种天然腔肠素的脱氧衍生物。当使用原水母发光蛋白时,腔肠素h的原始光输出量高于腔肠素的两倍;当使用水母萤光素酶时,腔肠素h的原始光输出量减少却有更长时间的持续性活跃。
【使用案例】
Charles R, Namkung Y, Cotton M, et al. βarrestin-Mediated Angiotensin II Signaling Controls the Activation of ARF6 and Endocytosis in Migration of Vascular Smooth Muscle Cells.[J]. Journal of Biological Chemistry, 2015.
Lahaie N, Kralikova M, Pr E L, et al. Post-endocytotic deubiquitination and degradation of the metabotropic γ-aminobutyric acid receptor by the ubiquitin specific protease 14.[J]. Journal of Biological Chemistry, 2016.
Beata J, Yuanyuan C, Tivadar O, et al. Disruption of Rhodopsin Dimerization with Synthetic Peptides Targeting an Interaction Interface.[J]. Journal of Biological Chemistry, 2015, 290(42):25728-44.
Gimenez L E, Baameur F, Vayttaden S J, et al. Salmeterol Efficacy and Bias in the Activation and Kinase-Mediated Desensitization of β2-Adrenergic Receptors[J]. Molecular pharmacology, 2015, 87(6): 954-964.
Hu J, Stern M, Gimenez L E, et al. A G Protein-Biased Designer G Protein-Coupled Receptor Useful for Studying the Physiological Relevance of Gq/11-Dependent Signaling Pathways.[J]. Journal of Biological Chemistry, 2016.
Giner X C, Cotnoir-White D, Mader S, et al. Selective ligand activity at Nur/retinoid X receptor complexes revealed by dimer-specific bioluminescence resonance energy transfer-based sensors.[J]. Faseb Journal, 2015, 29(10).
Lim J H, Park G C, Lee S M, et al. Surface-Tunable Bioluminescence Resonance Energy Transfer via Geometry-Controlled ZnO Nanorod Coordination[J]. Small, 2015, 11(28):3469-3475.
Robertson D N, Sleno R, Nagi K, et al. Design and construction of conformational biosensors to monitor ion channel activation: A prototype FlAsH/BRET-approach to Kir3 channels[J]. Environmental Modelling & Software, 2015, 8(9):A21.
Nakajima K I, Gimenez L E D, Gurevich V V, et al. Design and Analysis of an Arrestin-Biased DREADD[J]. Neuromethods, 2015, 108:29-48.
Lee J, Ghil S. Regulator of G protein signaling 8 inhibits protease-activated receptor 1/Gi/o signaling by forming a distinct G protein-dependent complex in live cells.[J]. Cellular Signalling, 2016, 28(5):391-400.
Zhao P, Lieu T, Barlow N, et al. Neutrophil elastase activates PAR2 and TRPV4 to cause inflammation and pain.[J]. Journal of Biological Chemistry, 2015.
Guixà-González R, Javanainen M, Gómez-Soler M, et al. Membrane omega-3 fatty acids modulate the oligomerisation kinetics of adenosine A2Aand dopamine D2receptors[J]. Scientific Reports, 2015, 6.
Chen Y, Hong T. High-throughput screening assays to identify small molecules preventing photoreceptor degeneration caused by the rhodopsin P23H mutation.[M]// Rhodopsin. Springer New York, 2015:369-390.
4. Coelenterazine native 天然腔肠素
【产品货号】cat#303、CAS#55779-48-1
【产品规格】500µg、1mg、5mg、10mg
【产品简介】腔肠素游离碱,纯度>95%。它是自然界最丰富的腔肠素,是海肾萤光素酶的首选底物。
【使用案例】
Franchi F, Peterson K M, Paulmurugan R, et al. Noninvasive Monitoring of the Mitochondrial Function in Mesenchymal Stromal Cells[J]. Molecular Imaging & Biology, 2016:1-9.
Yukiko H, Shuko T, Hansang C, et al. A Food and Drug Administration-approved asthma therapeutic agent impacts amyloid β in the brain in a transgenic model of Alzheimer disease.[J]. Journal of Biological Chemistry, 2015, 290(4):1966-1978.
Markova S V, Larionova M D, Burakova L P, et al. The smallest natural high-active luciferase: Cloning and characterization of novel 16.5-kDa luciferase from copepod Metridia longa[J]. Biochemical & Biophysical Research Communications, 2015, 457(1):77-82.
Abu‐Hayyeh S, Ovadia C, Lieu T M, et al. Prognostic and mechanistic potential of progesterone sulfates in intrahepatic cholestasis of pregnancy and pruritus gravidarum[J]. Hepatology, 2015.
Daniel W. Stuckey †, Shawn D. Hingtgen †, Karakas N, et al. Engineering Toxin-Resistant Therapeutic Stem Cells to Treat Brain Tumors[J]. Stem Cells, 2015, 33(2):589-600.
Duo X, Yang Z, Yanfeng Q, et al. Androgen Receptor Splice Variants Dimerize to Transactivate Target Genes.[J]. Cancer Research, 2015, 75(17):3663-71.
Zhang X, Ao Z, Bello A, et al. Characterization of the inhibitory effect of an extract of Prunella vulgaris on Ebola virus glycoprotein (GP)-mediated virus entry and infection.[J]. Antiviral Research, 2016, 127:20-31.
Piret J, Goyette N, Eckenroth B E, et al. Contrasting effects of W781V and W780V mutations in helix N of herpes simplex virus 1 and human cytomegalovirus DNA polymerases on antiviral drug susceptibility.[J]. Journal of Virology, 2015, 89(8):4636-4644.
A R Hacobian, K Posa-Markaryan, S Sperger, et al. Improved osteogenic vector for non-viral gene therapy[J]. European cells & materials, 2016, 31:191-204.
Savolainen M H, Xu Y, My?H?Nen T T, et al. Prolyl Oligopeptidase Enhances α-Synuclein Dimerization via Direct Protein-Protein Interaction.[J]. Journal of Biological Chemistry, 2015, 290(8):5117-26.
Leroy E, Defour J P, Sato T, et al. His499 Regulates Dimerization and Prevents Oncogenic Activation by Asparagine Mutations of the Human Thrombopoietin Receptor.[J]. Journal of Biological Chemistry, 2015, 20(2):268-279.
5. Coelenterazine 400a 腔肠素400a
【产品货号】cat#340、CAS#70217-82-2
【产品规格】500µg、1mg、10mg
【产品简介】可以被水母萤光素酶(Rluc)氧化,但不能被海肾萤光素酶氧化。它适用于实时检测钙离子、基因报告子实验以及BRET的首选底物。这种衍生物的最大激发波长约400nm,因此对对绿色荧光蛋白接收器的干扰最小。
【使用案例】
Namkung Y, Radresa O, Armando S, et al. Quantifying biased signaling in GPCRs using BRET-based biosensors[J]. Methods, 2015, 92:5-10.
6. GLuc GLOW Assay kit 海肾萤光素酶活性分析试剂盒
【产品货号】cat#320
【产品规格】50ml (约1000个反应)
【产品简介】它是一种新型的一步法GLOW分析试剂盒,适用于高通量筛选(HTS)。这种试剂盒包含一种能够延长Gaussia信号超过几个小时的缓冲液,Gaussia的半衰期在2-3小时之间。它的优势包括:一步法分析试剂(单一溶液包含裂解、稀释和反应缓冲液)、稳定的发光信号(2-3小时的半衰期)、检测分泌型Gaussia萤光素酶、检测胞内表达的Gaussia萤光素酶,以及低背景(高信号比)。
【使用案例】
Si C, Zhang Z, Wu Y, et al. Endoplasmic Reticulum Stress and Store-Operated Calcium Entry Contribute to Usnic Acid-Induced Toxicity in Hepatic Cells.[J]. Toxicological Sciences An Official Journal of the Society of Toxicology, 2015, 146(1).
7. Firefly Luciferin free acid 萤火虫荧光素游离酸
【产品货号】cat#306、CAS#2591-17-5
【产品规格】250mg、500mg、1g
【产品简介】纯度99%,这是一种游离酸,而不是钾盐或者钠盐等水溶性盐,需要使用碱性缓冲液溶解。
【使用案例】
Camille Saini †, Volodymyr Petrenko †, Pamela Pulimeno †, et al. A functional circadian clock is required for proper insulin secretion by human pancreatic islet cells[J]. Diabetes Obesity & Metabolism, 2015.
Tien-Jen L, Wen-Miin L, Pei-Wen H, et al. Rapamycin Promotes Mouse 4T1 Tumor Metastasis that Can Be Reversed by a Dendritic Cell-Based Vaccine.[J]. Plos One, 2015, 10(10).
Chang W T, Lai T H, Chyan Y J, et al. Specific Medicinal Plant Polysaccharides Effectively Enhance the Potency of a DC-Based Vaccine against Mouse Mammary Tumor Metastasis.[J]. Plos One, 2015, 10(3).
Lin T J, Lin H T, Chang W T, et al. Shikonin-enhanced cell immunogenicity of tumor vaccine is mediated by the differential effects of DAMP components[J]. Molecular Cancer, 2015, 14(1):1-13.
8. Coenzyme A 辅酶A
【产品货号】cat#309、CAS#85-61-0、PubMed#6816
【产品规格】250mg、500mg、1g
【产品简介】腺苷-3-磷酸-5-二磷酸-泛酸酯(还原型),能够延长萤火虫萤光素酶生物发光信号。
【使用案例】
Paul Friedman K, Watt ED, Hornung MW, et al. Tiered High-Throughput Screening Approach to Identify Thyroperoxidase Inhibitors within the ToxCast Phase I and II Chemical Libraries.[J]. Toxicological Sciences, 2016.
9. Firefly Luc Assay Reagent 萤火虫萤光素酶分析试剂
【产品货号】cat#318
【产品规格】100ml
【产品简介】一步法萤光素酶分析试剂盒,适用于检测萤火虫萤光素酶检测,尤其是高通量筛选中的萤光素酶活性检测。1000个反应。具有最明亮的信号强度,最好的信号稳定性。
【使用案例】
Sundeep M, Dolan T M, Maben Z J, et al. Adrenocorticotropic Hormone (ACTH) Responses Require Actions of the Melanocortin-2 Receptor Accessory Protein on the Extracellular Surface of the Plasma Membrane.[J]. Journal of Biological Chemistry, 2015, 290(46):27972-85.
Malik S, Dolan T M, Maben Z J, et al. ACTH Responses Require Actions of the Melanocortin-2 Receptor Accessory Protein on the Extracellular Surface of the Plasma Membrane.[J]. Journal of Biological Chemistry, 2015, 290(Suppl3):103-103(1).
10. Polyclonal Antisera-Gluc 萤光素酶多克隆抗血清
【产品货号】cat#401P
【产品规格】250 µl
【产品简介】Gaussia萤光素酶的多克隆兔抗体,效价>1:10,000。
【使用案例】
Farideh M G, Church D R, Schreiber C L, et al. Inhibitor of p52 NF-κB subunit and androgen receptor (AR) interaction reduces growth of human prostate cancer cells by abrogating nuclear translocation of p52 and phosphorylated ARser81[J]. Genes & Cancer, 2015, 6(9-10):428-444.
11. Coelenterazine F 腔肠素F
【产品货号】cat#345、CAS#123437-16-1
【产品规格】500µg、1mg、10mg
【产品简介】腔肠素F是原水母发光蛋白的首选底物。
【使用案例】
Malikova N P, Borgdorff A J, Vysotski E S. Semisynthetic photoprotein reporters for tracking fast Ca(2+) transients.[J]. Photochemical & Photobiological Sciences, 2015, 14(12).
订购链接:http://www.bioconsumable.com/tools/search.asp?kw2=%C7%BB%B3%A6%CB%D8&tn=5
本文链接: http://bindingsite.immuno-online.com/view-1479783180.html