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Lentiviral Vector Equipment & Supplies

8 equipment items found

Lentiviral Vector (LVV) Therapy

Lentiviral Vector (LVV) Therapy

Manufactured by:Rocket Pharmaceuticals, Inc.   based inCranbury, NEW JERSEY (USA)
The process involves collection and isolation of a patient’s hematopoietic stem cells (HSCs), insertion of the corrected gene into the HSCs via a lentiviral vector outside the body, and the infusion of modified HSCs back into the patient. The goal is to enable sufficient quantities of a healthy, disease-modifying therapeutic protein to be manufactured by ...
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Premade Lentivirus for Lentiviral Vector Transduction

Premade Lentivirus for Lentiviral Vector Transduction

Manufactured by:Cellomics Technology, LLC   based inHalethorpe, MARYLAND (USA)
Lentiviral vector transduction is a powerful tool for delivering target genes into almost all types of dividing and non-dividing mammalian cells. Lentiviral vector can stably integrate into the host genome, allowing long-term stably, high-level gene expression both in vitro and in vivo. ...
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Lentivirus - Non-Replicating Lentiviral Vector

Lentivirus - Non-Replicating Lentiviral Vector

Manufactured by:Genenta Science   based inMilano, ITALY
After apheresis collection, a functional copy of the therapeutic gene is inserted into the patient’s own HSPCs using a non-replicating lentiviral vector. This is an ex-vivo process called transduction. We believe that LVVs are the first choice for ex-vivo gene therapy in humans because they can efficiently transduce HSPCs with potentially large transgenes ...
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Adeno-Associated Viral Vector (AAV) Therapy

Adeno-Associated Viral Vector (AAV) Therapy

Manufactured by:Rocket Pharmaceuticals, Inc.   based inCranbury, NEW JERSEY (USA)
The process involves collection and isolation of a patient’s hematopoietic stem cells (HSCs), insertion of the corrected gene into the HSCs via a lentiviral vector outside the body, and the infusion of modified HSCs back into the patient. The goal is to enable sufficient quantities of a healthy, disease-modifying therapeutic protein to be manufactured by ...
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Model SORT-C01 - pLV-H1TetO-GFP-Puro

Model SORT-C01 - pLV-H1TetO-GFP-Puro

Manufactured by:Biosettia Inc.    based inSan Diego, CALIFORNIA (USA)
Inducible pLV-RNAi vector system is designed to deliver gene silencing in a tightly regulated fashion in mammalian cell lines. The shRNA expression is suppressed by Tet repressor (TetR) binding to the hybrid H1 promoter containing tetracycline operators (TetO) and RNA interference only takes place in the presence of tetracycline. The inducible RNAi system provides the option of expressing shRNA ...
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Lenti-X - Model SARS-CoV-2 - Universal Pseudovirus Packaging Systems

Lenti-X - Model SARS-CoV-2 - Universal Pseudovirus Packaging Systems

Manufactured by:DSS Takara Bio India Pvt Ltd   based inNew Delhi, INDIA
Lenti-X SARS-CoV-2 Packaging Single Shots (Universal) gives you the flexibility to easily produce high-titer lentivirus pseudotyped with any SARS-CoV-2 spike variant desired. Simply clone any desired SARS-CoV-2 spike variant sequence into the provided expression vector, dilute in sterile water with your transfer vector of choice, and add to a tube of single shots. Then, apply the reconstituted ...
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OriGene - Lentivirus shRNA, Plasmids and Ientiviral Particles

OriGene - Lentivirus shRNA, Plasmids and Ientiviral Particles

Manufactured by:OriGene Technologies, Inc.   based inRockville, MARYLAND (USA)
OriGene offers pre-made lentiviral shRNA plasmid kits containing 4 sequence-verified expression cassettes that target your gene of interest. Each lentiviral cassette contains three major functional elements: shRNA, a puromycin selection marker & a tGFP reporter. With a guaranteed knockdown of ≥70%, these kits and our ready-to-use lenti-shRNA particles are a great option for studying ...
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Fanconi Anemia (FA)

Fanconi Anemia (FA)

Manufactured by:Rocket Pharmaceuticals, Inc.   based inCranbury, NEW JERSEY (USA)
FA is a rare, genetic disorder affecting DNA repair. Approximately two-thirds of FA cases are caused by genetic defects in the FANCA gene, which results in the FA subtype known as FA Complementation Group A (FA-A). FA patients may develop bone marrow failure (very low blood counts), cancers of the blood or other ...
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