product summary
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company name :
MyBioSource
product type :
other
product name :
QuickTiter HIV Lentivirus Quantitation Kit (p24 ELISA)
catalog :
MBS168758
quantity :
96 Assays
price :
695 USD
more info or order :
image
image 1 :
MyBioSource MBS168758 image 1
image 2 :
MyBioSource MBS168758 image 2
product information
catalog number :
MBS168758
products type :
Assay Kit
products full name :
QuickTiter HIV Lentivirus Quantitation Kit (p24 ELISA)
products short name :
[QuickTiter HIV Lentivirus (p24 ELISA)]
products name syn :
[QuickTiter HIV Lentivirus Quantitation Kit (p24 ELISA)]
storage stability :
Upon receiving, aliquot and store recombinant HIV-1 p24 Standard at -20 degree C and avoid freeze/thaw. Store all other components at 4 degree C until their expiration dates.
image1 heading :
Testing Data
image2 heading :
Testing Data #2
products categories :
Viral Expression; Lentivrial Expresion; Lentivirus Quantitation / Titer; Traditional p24 ELISA Kit
products description :
Principle of the assay: An anti-HIV p24 monoclonal coating antibody is adsorbed onto a microtiter plate. p24 antigen present in the sample or standard binds to the antibodies adsorbed on the plate; a FITC-conjugated mouse anti-p24 antibody is added and binds to p24 antigen captured by the first antibody. Following incubation and wash steps, a HRP-conjugated mouse anti-FITC antibody is added and binds to the FITC conjugated anti-p24. Following unbound HRP-conjugated mouse anti-FITC antibody is removed during a wash step, and substrate solution reactive with HRP is added to the wells. A colored product is formed in proportion to the amount of p24 antigen present in the sample. The reaction is terminated by addition of acid and absorbance is measured at 450 nm. A standard curve is prepared from recombinant HIV-1 p24 protein and sample p24 concentration is then determined. Background: Lentivirus vector based on the human immunodeficiency virus-1 (HIV-1) has become a promising vector for gene transfer studies. The advantageous feature of lentivirus vector is the ability of gene transfer and integration into dividing and non-dividing cells1-2. The pseudotyped envelope with vesicular stomatitis virus envelope G (VSV-G) protein broadens the target cell range. Lentiviral vectors have been shown to deliver genes to neurons, lymphocytes and macrophages, cell types that previous retrovirus vectors could not be used. Lentiviral vectors have also proven to be effective in transducing brain, liver, muscle, and retina in vivo without toxicity or immune responses. Recently, the lentivirus system is widely used to integrate siRNA efficiently in a wide variety of cell lines and primary cells both in vitro and in vivo. Lentivirus particles are produced from 293T cells through transient transfection of 3 or 4 plasmids that encodes for the components of the virion. Viral medium containing viral particles produced by packaging cells within 48-72 hr can be harvested. To ensure that pseudoviral medium is viable, and to control the number of copies of integrated viral constructs per target cell, the viral titer needs to be determined before proceeding with transduction experiments. Viral titer can be determined by transduction of HT-1080 or HeLa cells, and followed by antibiotic selection of stable clones. However, it takes weeks to generate sizable stable cell colonies for counting and calculating the titer results. QuickTiter HIV Lentiviral Quantitation Kit (HIV p24 ELISA) is an enzyme immunoassay developed for detection and quantitation of the HIV-1 p24 core protein. A mouse monoclonal antibody to HIV-1 p24 is coated onto strip wells of microtiter plate. The quantity of HIV p24 antigen is determined by comparing its absorbance with that of known recombinant p24 antigen standard curve. The kit has a detection sensitivity limit of 1 ng/mL HIV p24, or about 10,000 to 100,000 TU/mL VSVG-pseudotyped lentivirus samples3-5. Each kit provides sufficient reagents to perform up to 96 assays including standard curve and unknown samples. The kit is suitable for both viral supernatant and purified virus. The QuickTiter HIV Lentiviral Quantitation Kit is intended for research use only, and not for diagnostic applications.
products references :
1. Naldini, L., U. Blomer, P. Gallay, D. Ory, R. Mulligan, F. H. Gage, I. M. Verma, and D. Trono (1996) Science 272, 263-267. 2. Verma, I. M., and N. Somia (1997) Nature 389, 239-242. 3. Kahl C. A., Marsh J., Fyffe J., Sanders D. A., and K. Cornetta (2004) J Virol. 78:1421-30. 4. White S. M., Renda M., Nam N. Y., Klimatcheva E., Zhu Y., Fisk J., Halterman M., Rimel B. J., Federoff H., Pandya S., Rosenblatt J. D., and V. Planelles (1999) J Virol. 73:2832-40. 5. Kafri T., van Praag H., Ouyang L., Gage F. H., and I. M. Verma (1999) J Virol. 73:576-84. 1. Lucera, M.B. et al. (2014). The Histone Deacetylase Inhibitor Vorinostat (SAHA) Increases the Susceptibility of Uninfected CD4+ T Cells to HIV by Increasing the Kinetics and Efficiency of Postentry Viral Events. J Virol. 88:10803-10812. 2. Tabler, C.O. et al. (2014). CD4+ Memory Stem Cells Are Infected by HIV-1 in a Manner Regulated in Part by SAMHD1 Expression. J Virol. 88:4976-4986. 3. Mincheva-Tasheva, S. (2014). Apoptotic cell death and altered calcium homeostasis caused by frataxin depletion in dorsal root ganglia neurons can be prevented by BH4 domain of Bcl-xL protein. Hum. Mol. Genet. 23:1829-1841. 4. Yi, S.H. et al. (2014). Foxa2 Acts as a Co-Activator Potentiating Expression of the Nurr1-Induced DA Phenotype via Epigenetic Regulation. Development. 141:761-772. 5. Tasheva, S. et al. (2013). Apoptotic cell death and altered calcium homeostasis caused by frataxin depletion in dorsal root ganglia neurons can be prevented by BH4 domain of Bcl-xL protein. Human. Mol. Genet. 10.1093/hmg/ddt576. 6. Kong, L. et al. (2013). Interferon Alfa Partially Inhibits HIV Replication in Hepatocytes In Vitro. The Journal of Infectious Disease. 99:632-639. 7. Smith, B. et al. (2013). Targeting the PyMT Oncogene to Diverse Mammary Cell Populations Enhances Tumor Heterogeneity and Generates Rare Breast Cancer Subtypes. Genes & Cancer. 10.1177/1947601913475359. 8. Iftikhar, M. et al. (2011). Lysyl Oxidase-like-2 (LOXL2) is a Major Isoform in Chondrocytes and is Critically Required for Differentiation. J. Biol. Chem. 286:909-918. 9. Piedrahita, D. et al. (2010). Silencing of CDK5 Reduces Neurofibrillary Tangles in Transgenic Alzheimer's Mice. J. Neurosci. 30:13966-13976.10. Agrawai-Gamse, C. et al. (2010). Yeast-elicited cross-reactive antibodies to HIV Env glycans efficiently neutralize virions expressing exclusively high-mannoseN-Linked glycans. J. Virol. 10.1128/JVI.01349-10. 11. Young, A.P. and Wagers, A.J. (2010). Pax3 induces differentiation of juvenile skeletal muscle stem cells without transcriptional upregulation of canonical myogenic regulatory factors. J. Cell Sci. 123: 2632-2639. 12. Kaletsky, R. et al. (2009). Tetherin-mediated restriction of filovirus budding is antagonized by the Ebola glycoprotein. PNAS 106:2886-2891. 13. Krishnamachary, B. et al. (2009). Noninvasive detection of lentiviral-mediated choline kinase targeting in a human breast cancer xenograft. Cancer Res. 69:3464-3471. 14. Malur, A. et al. (2009). Deletion of PPAR-gamma in alveolar macrophages is associated with Th-1 pulmonary inflammatory response. J. Immunol. 182:5816-5822. 15. Shu, L and P.J. Houghton (2009). The mTORC2 complex regulates terminal differentiation of C2C12 myoblasts. Mol. Cell. Biol. 29:4691-4700. 16. Agrawal-Gamse, C. et al. (2009). Adaptive mutations in a V3-truncated HIV-1 envelope restore function by improving interactions with CD4. J. Virol. 10.1128/JVI.01238-09. 17. Lambert, M.P. et al. (2009). Platelet factor 4 regulates megakaryopoiesis through low density lipoprotein receptor related protein 1 (LRP1) on megakaryocytes. Blood 114:2290-2298. 18. Brittain, J.M. et al. (2009). An atypical role for collapsin response mediator protein (CRMP-2) in neurotransmitter release via interaction with presynaptic voltage-gated calcium channels. J. Biol. Chem. 284:31375-31390. 19. Wilson, A.A. et al. (2008). Sustained expression of alpha-1 antitrypsin after transplantation of manipulated hematopoietic stem cells. Am. J. Respir. Cell Mol. Biol. 39:133-141. 20. Thomassen, M.J. et al. (2007). ABCG1 is deficient in alveolar macrophages of GM-CSF knock-out mice and patients with pulmonary alveolar proteinosis. J. Lipid Res. 48:2762-2768. 21. Sadat, S. et al. (2007). The cardioprotective effect of mesenchymal stem cells is mediated by IGF-I and VEGF. Biochem. and Biophys. Res. Comm. 363:674-679. 22. Apolonia, L. et al. (2007). Stable gene transfer to muscle using non-integrating lentiviral vectors. Mol. Ther. 15:1947-1954.
size1 :
96 Assays
price1 :
695 USD
size2 :
5x96 Assays
price2 :
2810
more info or order :
company information
MyBioSource
P.O. Box 153308
San Diego, CA 92195-3308
sales@mybiosource.com
https://www.mybiosource.com
1-888-627-0165
headquarters: USA
MyBioSource, LLC was orginally founded in Vancouver by three enthusiastic scientists who are passionate about providing the world with the best reagents available. Together, they form a company with a big vision known as MyBioSource. MyBioSource is now located in San Diego, California, USA.

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