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商品详细Athens Research/Cambio - Excellence in Molecular Biology/250 tests/11-1250
Athens Research/Cambio - Excellence in Molecular Biology/250 tests/11-1250
Athens Research/Cambio - Excellence in Molecular Biology/250 tests/11-1250
商品编号: 11-1250
市场价: ¥0.00
美元价: 0.00
产地: 美国(厂家直采)
公司:
产品分类: 多肽合成
公司分类: peptide
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍
Cell culture contamination control

Cell culture contamination control: Detection

Detection and identification of Mycoplasma

  • Catalogue
  • Description
  • Protocols
  • References
  • Notes

Venor®GeM Classic Mycoplasma PCR Detection Kit

Venor®GeMMycoplasma PCR Detection Kit for rapid and reliable detection of mycoplasma in various in situ biologicals including cell cultures and virus stocks

Minerva Biolabs

Catalogue No.DescriptionPack SizePriceQty
  • Change to:
  • €
11-1025Venor®GeM Classic Mycoplasma PCR Detection Kit25 tests£125.00QuantityAdd to Order
11-1050Venor®GeM Classic Mycoplasma PCR Detection Kit50 tests£221.00QuantityAdd to Order
11-1100Venor®GeM Classic Mycoplasma PCR Detection Kit100 tests£387.00QuantityAdd to Order
11-1250Venor®GeM Classic Mycoplasma PCR Detection Kit250 tests£831.00QuantityAdd to Order
11-1905Venor®GeM extra internal control DNA4 vials£19.00QuantityAdd to Order

Venor®GeM Classic Mycoplasma PCR Detection Kit

Venor®GeMMycoplasma PCR Detection Kit for rapid and reliable detection of mycoplasma in various in situ biologicals including cell cultures and virus stocks

Minerva Biolabs

Venor®GeM Classic

Venor®GeM Classic allows fast, reliable and time-saving routine monitoring of mycoplasma contamination by PCR.

Type of PCR

For conventional, endpoint PCR

Recommended Use / Scope

Applicable in research and industry for direct testing of cell cultures and biologicals. Intended for research use only. Not recommended for clinical diagnostics.

Kit Components

Lyophilized primer sets and nucleotides 10x reaction buffer optimized for MB Taq DNA Polymerase Lyophilized positive control DNA Lyophilized internal amplification control

Package Sizes

Primer sets and nucleotides are prepared in aliquots of 25 tests.

  • Cat. No. 11-1025 25 Tests
  • Cat. No. 11-1050 50 Tests
  • Cat. No. 11-1100 100 Tests
  • Cat. No. 11-1250 250 Tests

Result evaluation

Gel electrophoresis at endpoint of PCR

Required Consumables

Polymerase. We highly recommend our reliable hot-start MB Taq DNA Polymerase, Cat.-No. 53-0050/100/200/250. PCR reaction tubes

Optional for process validation and EP 2.6.7 compliant testing: Internal Control DNA extra (4 vials for 300 µl each of internal amplification control; Cat. No. 11-1905) 10CFU™ Sensitivity Standards available for all EP listed mycoplasma species

Required lab devices

Regular PCR cycler Agarose gel electrophoresis and DNA staining system Pipetting equipment Tube centrifuge

Shelf Life and Storage

Components are maintainable at2 to8 °C for at least 6 months. After rehydratisation the reagents must be stored at -18 °C.

EP 2.6.7 compliance

Use of Venor®GeM Classic for QA testing of biologicals like master and working cell banks, autologous cells, culture media, bulk harvest and final product testing according to EP 2.6.7 is applicable after appropriate sample preparation and process validation.

Fig. Amplified PCR products are visualized by standard gel electrophoresis.

If you cannot find the answer to your problem below then please contact us or telephone 01954 210 200

Venor®GeM Classic Mycoplasma PCR Detection Kit

Venor®GeMMycoplasma PCR Detection Kit for rapid and reliable detection of mycoplasma in various in situ biologicals including cell cultures and virus stocks

Minerva Biolabs

You can find your Venor®GeM Classic protocols here:

Click to download:

Venor®GeM Classic Kit Full Protocol

alternatively,

if you are in a rush click to view:

Venor®GeM Classic Kit Quick Visual Guide

If you cannot find the answer to your problem below then please contact us or telephone 01954 210 200

Venor®GeM Classic Mycoplasma PCR Detection Kit

Venor®GeMMycoplasma PCR Detection Kit for rapid and reliable detection of mycoplasma in various in situ biologicals including cell cultures and virus stocks

Minerva Biolabs

Venor®GeM Mycoplasma Detection Kits

Anugraham M. et al., (2014). Specific Glycosylation of Membrane Proteins in Epithelial Ovarian Cancer Cell Lines: Glycan Structures Reflect Gene Expression and DNA Methylation Status. Molecular & Cellular Proteomics, 13(9):2213-32. doi: 10.1074/mcp.M113.037085

Brinzeu D.G.T. et al., (2008). Microbial and Fungal Contamination of Keratinocyte and Fibroblast Cell Cultures. Journal of Experimental Medical & Surgical Research, 3 / 123 – 128.

Chal J. et al., (2016). Generation of human muscle fibers and satellite-like cells from human pluripotent stem cells in vitro. Nature Protocols 11(10):1833-50. doi: 10.1038/nprot.2016.110.

Dzieran J. et al., (2013). Comparative Analysis of TGF-β/Smad Signaling Dependent Cytostasis in Human Hepatocellular Carcinoma Cell Lines. PLoS One, 8(8):e72252. doi: 10.1371/journal.pone.0072252.

Falagan-Lotsch P.et al., (2015). Performance of PCR-based and bioluminescent assays for mycoplasma detection. Journal of Microbiological Methods, 118:31-6. doi: 10.1016/j.mimet.2015.08.010.

Gutzeit C.et al., (2014). Exosomes derived from Burkitt"s lymphoma cell lines induce proliferation, differentiation, and class-switch recombination in B cells. Journal of Immunology, 192(12):5852-62. doi: 10.4049/jimmunol.1302068.

Henrich B.et al., (2010). Mycoplasma salivarium detected in a microbial community with Candida glabrata in the biofilm of an occluded biliary stent. Journal of Medical Microbiology, 59, 239–241. doi: 10.1099/jmm.0.013110-0.

Loring J.F., Wesselschmidt R.L., and Schwartz P.H. (2007). Human Stem Cell Manual: A Laboratory Guide.Elsevier Inc.

Maass V.et al., (2011). Sequence homologies between Mycoplasma and Chlamydia spp. lead to false-positive results in chlamydial cell cultures tested for mycoplasma contamination with a commercial PCR assay. Journal of Clinical Microbiology, 49(10):3681-2. doi: 10.1128/JCM.01092-11.

Malenovska H. and Reichelova M., (2011). Elimination of mycoplasma contamination of virus stocks.Veterinarni Medicina, 56 (11): 547–550.

Mudduluru G.et al., (2015). A Systematic Approach to Defining the microRNA Landscape in Metastasis. Cancer Research, 75(15). doi: 10.1158/0008-5472.CAN-15-0997.

Nübling C.M.et al., (2015). World Health Organization International Standard to Harmonize Assays for Detection of Mycoplasma DNA. Applied and Environmental Microbiology, 81(17):5694-702. doi: 10.1128/AEM.01150-15.

Oksvold M.P.et al., (2012). Effect of cycloheximide on epidermal growth factor receptor trafficking and signaling. FEBS Letters, 586(20):3575-81. doi: 10.1016/j.febslet.2012.08.022.

Pandrangi S.L.et al., (2014). Establishment and characterization of two primary breast cancer cell lines from young Indian breast cancer patients: mutation analysis. Cancer Cell International, 14(1):14. doi: 10.1186/1475-2867-14-14.

Panosa C. et al., (2013). Development of an Epidermal Growth Factor Derivative with EGFR Blocking Activity. PLoS One, 8(7):e69325. doi: 10.1371/journal.pone.0069325.

Pérez-Garay M. et al., (2010). 2,3-Sialyltransferase ST3Gal III Modulates Pancreatic Cancer Cell Motility and Adhesion In Vitro. PLoS One, 5(9): e12524. doi: 10.1371/journal.pone.0012524.

Picco G. et al., (2017). Loss of AXIN1 drives acquired resistance to WNT pathway blockade in colorectal cancer cells carrying RSPO3 fusions. EMBO Molecular Medicine, 9(3):293-303. doi: 10.15252/emmm.201606773.

Pietrosi G. et al., (2015). Phases I–II Matched Case-Control Study of Human Fetal Liver Cell Transplantation for Treatment of Chronic Liver Disease. Cell Transplantation, 24(8):1627-38. doi: 10.3727/ 096368914X682422.

Pontarin G. et al., (2006). Mitochondrial DNA Depletion and Thymidine Phosphate Pool Dynamics in a Cellular Model of Mitochondrial Neurogastrointestinal Encephalomyopathy. The Journal of Biological Chemistry, 281(32):22720-8. doi: 10.1074/jbc.M604498200.

Rappa G. et al., (2015). Ethanol induces upregulation of the nerve growth factor receptor CD271 in human melanoma cells via nuclear factor-κB activation. Oncology Letters, 10: 815-821. doi: 10.3892/ol.2015.3343.

Sajadian S.O. et al., (2016). Vitamin C enhances epigenetic modifications induced by 5-azacytidine and cell cycle arrest in the hepatocellular carcinoma cell lines HLE and Huh7. Clinical Epigenetics, 8:46. doi: 10.1186/s13148-016-0213-6.

Samanta D. et al., (2012). Smoking attenuates Transforming growth factor-β-mediated tumor suppression function through down-regulation of Smad3 in lung cancer. Cancer Prevention Research, 5(3): 453–463. doi:10.1158/1940-6207.

Schmitt M. et al., (2009). High-throughput detection and multiplex identification of cell contaminations. Nucleic Acids Research, 37(18):e119. doi:10.1093/nar/gkp581.

Smith C. (2005). Trouble in the hood: culturing difficult cell types.Nature Methods 2, 385–391. doi: 10.1038/nmeth0505-385

Thies A. et al., (2007). Clinically proven markers of metastasis predict metastatic spread of human melanoma cells engrafted in scid mice. British Journal of Cancer, 96(4):609-16. doi: 10.1038/sj.bjc.6603594.

Vickovic S. et al., (2016). Massive and parallel expression profiling using microarrayed single-cell sequencing. Nature Communications, 7:13182. doi: 10.1038/ncomms13182.

Waddington R.J. and Sloan A.J. (2017). Tissue Engineering and Regeneration in Dentistry – Current Strategies.John Wiley & Sons, Ltd.

Winter S. et al., (2016). Methylomes of renal cell lines and tumors or metastases differ significantly with impact on pharmacogenes. Scientific Reports, 6:29930. doi: 10.1038/srep29930.

Wolff J. et al., (2013). GMP-level adipose stem cells combined with computer-aided manufacturing to reconstruct mandibular ameloblastoma resection defects: Experience with three cases. Annals of Maxillofacial Surgery, 3(2):114-25. doi: 10.4103/2231-0746.119216.

If you cannot find the answer to your problem below then please contact us or telephone 01954 210 200

Venor®GeM Classic Mycoplasma PCR Detection Kit

Venor®GeMMycoplasma PCR Detection Kit for rapid and reliable detection of mycoplasma in various in situ biologicals including cell cultures and virus stocks

Minerva Biolabs

Click here to download full product information.

If you cannot find the answer to your problem below then please contact us or telephone 01954 210 200

品牌介绍
Athens Research & Technology—供应多款蛋白、酶制品 Athens Research & Technology是成立于2010年的新兴生物高科技制品公司,该公司拥有BSL-2实验室及超过11000平方英尺的cGMP生产厂房,并且通过ISO 9001:2008认证。Athens公司致力于纯化分离高纯度,高活性的人类蛋白质及研发多克隆抗血清产品。提供包括高纯度及活性的丝氨酸蛋白酶,蛋白酶抑制剂,中性粒细胞酶,载脂蛋白,脂蛋白,血小板蛋白,转铁蛋白,免疫球蛋白等等。公司产品适用于炎症,冠状动脉疾病,自身免疫性疾病,癌症,阿尔茨海默氏病等众多研究领域,已被世界*制药公司及诊断试剂公司用于体外诊断试剂盒/免疫检测试剂盒、药物筛选、细胞培养液(包括干细胞)等产品研发。除了人类蛋白质,我们还从动物血清和组织中分离多种蛋白质及酶类。此外,Athens Research and Technology还提供特殊试剂/蛋白定制服务,以满足研究人员的不同需求。