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Product Image-10755-796

innuPREP Micro RNA Kit , Analytik Jena

Supplier: Analytik Jena US
Description: The innuPREP Micro RNA Kit allows researchers to isolate small RNA molecules and achieve high yields.

Product Image-76004-168

Zymo-Spin™ VE Columns, Zymo Research

Supplier: Zymo Research
Description: Spin columns for the purification of DNA or RNA.

Image Unavailable-10325-092

Anti-ADAR Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (10325-092)
Supplier: Bioss
Description: Catalyzes the hydrolytic deamination of adenosine to inosine in double-stranded RNA (dsRNA) referred to as A-to-I RNA editing. This may affect gene expression and function in a number of ways that include mRNA translation by changing codons and hence the amino acid sequence of proteins; pre-mRNA splicing by altering splice site recognition sequences; RNA stability by changing sequences involved in nuclease recognition; genetic stability in the case of RNA virus genomes by changing sequences during viral RNA replication; and RNA structure-dependent activities such as microRNA production or targeting or protein-RNA interactions. Can edit both viral and cellular RNAs and can edit RNAs at multiple sites (hyper-editing) or at specific sites (site-specific editing). Its cellular RNA substrates include: bladder cancer-associated protein (BLCAP), neurotransmitter receptors for glutamate (GRIA2) and serotonin (HTR2C) and GABA receptor (GABRA3). Site-specific RNA editing of transcripts encoding these proteins results in amino acid substitutions which consequently alters their functional activities. Exhibits low-level editing at the GRIA2 Q/R site, but edits efficiently at the R/G site and HOTSPOT1. Its viral RNA substrates include: hepatitis C virus (HCV), vesicular stomatitis virus (VSV), measles virus (MV), hepatitis delta virus (HDV), and human immunodeficiency virus type 1 (HIV-1). Exhibits either a proviral (HDV, MV, VSV and HIV-1) or an antiviral effect (HCV) and this can be editing-dependent (HDV and HCV), editing-independent (VSV and MV) or both (HIV-1). Impairs HCV replication via RNA editing at multiple sites. Enhances the replication of MV, VSV and HIV-1 through an editing-independent mechanism via suppression of EIF2AK2/PKR activation and function. Stimulates both the release and infectivity of HIV-1 viral particles by an editing-dependent mechanism where it associates with viral RNAs and edits adenosines in the 5'UTR and the Rev and Tat coding sequence.
Image Unavailable-10325-090

Anti-ADAR Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10325-090)
Supplier: Bioss
Description: Catalyzes the hydrolytic deamination of adenosine to inosine in double-stranded RNA (dsRNA) referred to as A-to-I RNA editing. This may affect gene expression and function in a number of ways that include mRNA translation by changing codons and hence the amino acid sequence of proteins; pre-mRNA splicing by altering splice site recognition sequences; RNA stability by changing sequences involved in nuclease recognition; genetic stability in the case of RNA virus genomes by changing sequences during viral RNA replication; and RNA structure-dependent activities such as microRNA production or targeting or protein-RNA interactions. Can edit both viral and cellular RNAs and can edit RNAs at multiple sites (hyper-editing) or at specific sites (site-specific editing). Its cellular RNA substrates include: bladder cancer-associated protein (BLCAP), neurotransmitter receptors for glutamate (GRIA2) and serotonin (HTR2C) and GABA receptor (GABRA3). Site-specific RNA editing of transcripts encoding these proteins results in amino acid substitutions which consequently alters their functional activities. Exhibits low-level editing at the GRIA2 Q/R site, but edits efficiently at the R/G site and HOTSPOT1. Its viral RNA substrates include: hepatitis C virus (HCV), vesicular stomatitis virus (VSV), measles virus (MV), hepatitis delta virus (HDV), and human immunodeficiency virus type 1 (HIV-1). Exhibits either a proviral (HDV, MV, VSV and HIV-1) or an antiviral effect (HCV) and this can be editing-dependent (HDV and HCV), editing-independent (VSV and MV) or both (HIV-1). Impairs HCV replication via RNA editing at multiple sites. Enhances the replication of MV, VSV and HIV-1 through an editing-independent mechanism via suppression of EIF2AK2/PKR activation and function. Stimulates both the release and infectivity of HIV-1 viral particles by an editing-dependent mechanism where it associates with viral RNAs and edits adenosines in the 5'UTR and the Rev and Tat coding sequence.
Product Image-76005-178

Zymo-Spin™ V Columns, Zymo Research

Supplier: Zymo Research
Description: Spin columns for the purification of DNA or RNA.

Image Unavailable-10204-748

MPure™ Total RNA Extraction Kit, MP Biomedicals

Catalog Number: (10204-748)
Supplier: MP Biomedicals
Description: MPure Total RNA Extraction Kit is used with the MPure-12 instrument for extraction of total RNA from whole blood, blood cells, animal tissue, plant tissue, yeast or cultured cells.
Product Image-76081-662

MasterPure™ Yeast RNA Purification Kit, Biosearch Technologies

Catalog Number: (76081-662)
Supplier: Lucigen
Description: Safe, fast purification of high quality RNA from multiple species of yeast
Product Image-97066-614

Total RNA Isolation Mini Kit, Agilent Technologies

Catalog Number: (97066-614)
Supplier: Agilent Technologies
Description: RNA isolation kits provide a straightforward, spin-column method to deliver RNA for use in gene expression and other downstream analysis.
Product Image-97060-572

gMAX Genomic DNA Kit, IBI Scientific

Supplier: IBI Scientific
Description: IBI's gMax MINI Genomic DNA Extraction/Purification Kit provides a fast and efficient method for purifying total DNA (including genomic, mitochondrial and viral DNA) from whole blood (fresh/frozen), tissue, buccal swab, and amniotic fluid

Product Image-76509-254

RNA-Solv® RNA Isolation, Reagent, Omega bio-tek

Catalog Number: (76509-254)
Supplier: Omega Bio-Tek
Description: RNA-Solv® Reagent is a one reagent system for the isolation of total RNA from cells and tissues. The reagent, a single-phase solution consisting of phenol and guanidine isothiocyanate, is a modification of the single-step RNA isolation method developed by Chomczynski and Sacchi. The sample is homogenised and lysed in RNA-Solv® Reagent, which maintains the integrity of the RNA while disrupting and denaturing endogenous RNases and other cellular components. Extraction of the lysate with chloroform further denatures proteins and separates the mixture into an organic and an aqueous phase. RNA remains exclusively in the aqueous phase, and is subsequently recovered by isopropanol.
Image Unavailable-103529-146

Monarch® RNA Purification Columns, New England Biolabs

Catalog Number: (103529-146)
Supplier: New England Biolabs (NEB)
Description: Need more RNA Purification Columns? No problem. NEB supplies all Monarch® kit components separately.
Product Image-10325-076

Anti-ADAR Rabbit Polyclonal Antibody

Catalog Number: (10325-076)
Supplier: Bioss
Description: Catalyzes the hydrolytic deamination of adenosine to inosine in double-stranded RNA (dsRNA) referred to as A-to-I RNA editing. This may affect gene expression and function in a number of ways that include mRNA translation by changing codons and hence the amino acid sequence of proteins; pre-mRNA splicing by altering splice site recognition sequences; RNA stability by changing sequences involved in nuclease recognition; genetic stability in the case of RNA virus genomes by changing sequences during viral RNA replication; and RNA structure-dependent activities such as microRNA production or targeting or protein-RNA interactions. Can edit both viral and cellular RNAs and can edit RNAs at multiple sites (hyper-editing) or at specific sites (site-specific editing). Its cellular RNA substrates include: bladder cancer-associated protein (BLCAP), neurotransmitter receptors for glutamate (GRIA2) and serotonin (HTR2C) and GABA receptor (GABRA3). Site-specific RNA editing of transcripts encoding these proteins results in amino acid substitutions which consequently alters their functional activities. Exhibits low-level editing at the GRIA2 Q/R site, but edits efficiently at the R/G site and HOTSPOT1. Its viral RNA substrates include: hepatitis C virus (HCV), vesicular stomatitis virus (VSV), measles virus (MV), hepatitis delta virus (HDV), and human immunodeficiency virus type 1 (HIV-1). Exhibits either a proviral (HDV, MV, VSV and HIV-1) or an antiviral effect (HCV) and this can be editing-dependent (HDV and HCV), editing-independent (VSV and MV) or both (HIV-1). Impairs HCV replication via RNA editing at multiple sites. Enhances the replication of MV, VSV and HIV-1 through an editing-independent mechanism via suppression of EIF2AK2/PKR activation and function. Stimulates both the release and infectivity of HIV-1 viral particles by an editing-dependent mechanism where it associates with viral RNAs and edits adenosines in the 5'UTR and the Rev and Tat coding sequence.
Product Image-76081-774

QuickExtract™ RNA Extraction Solution, RT-PCR-ready RNA, Biosearch Technologies

Catalog Number: (76081-774)
Supplier: Lucigen
Description: Rapid, simple RNA extraction (no purification) from mammalian cells, ready for RT-PCR applications
Product Image-76020-646

Direct-zol™ RNA Pre-Wash, Zymo Research

Supplier: Zymo Research
Description: Designed for use with Direct-zol™ RNA MiniPrep Purification Kits.

Product Image-76004-154

Zymo-Spin™ IB Columns, Zymo Research

Supplier: Zymo Research
Description: Spin columns for the purification of DNA and/or RNA and fluorescent dye removal.

Product Image-99901-386

AdEasy Virus Purification Kit, Agilent Technologies

Catalog Number: (99901-386)
Supplier: Agilent Technologies
Description: The AdEasy Virus Purification Kit allows the purification and concentration of Adenovirus (from Ad5 strains) with Sartobind® syringe filters containing an ion exchange membrane adsorber that selectively binds adenoviral particles. Once bound, viral particles can be further purified by washing away nonspecifically-bound proteins before elution. Concentrated and purified viral particles can be obtained in 2 to 3 hours, in contrast to traditional CsCl gradient centrifugation which typically takes 12 to 48 hours.
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
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