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G413317-25mg
Glecaprevir (C007B-173386)
Price: $314.08List Price: $348.98InformationGlecaprevir Glecaprevir is a hepatitis C virus (HCV) nonstructural (NS) protein 3/4A protease inhibitor that targets the the viral RNA replication. It displays IC50 values ranging from 3.5 to 11.3 nM for clinical isolates of HCV genotypes -
G413317-50mg
Glecaprevir (C007B-173387)
Price: $492.33List Price: $547.03InformationGlecaprevir Glecaprevir is a hepatitis C virus (HCV) nonstructural (NS) protein 3/4A protease inhibitor that targets the the viral RNA replication. It displays IC50 values ranging from 3.5 to 11.3 nM for clinical isolates of HCV genotypes -
G413317-5mg
Glecaprevir (C007B-173388)
Price: $112.33List Price: $124.81InformationGlecaprevir Glecaprevir is a hepatitis C virus (HCV) nonstructural (NS) protein 3/4A protease inhibitor that targets the the viral RNA replication. It displays IC50 values ranging from 3.5 to 11.3 nM for clinical isolates of HCV genotypes -
RP018-01
Herpes Simplex Virus Type I Polyclonal Antibody, 100 L, Liquid
Price: $920.43List Price: $1,022.70Background The herpes simplex (HSV) (also known as cold sore, night fever or fever blister) is a virus that causes a contagious disease. There are two main types of Herpes Simplex Virus (HSV) , 1 and 2 and they belong to a family that includes -
GE17372212
HITRAP(R) CAPTO(TM) AVB 1X5 ML GE HEALTHCARE
Price: $3,416.58List Price: $3,796.20Capto AVB is based on a rigid base matrix, delivering excellent pressure-flow properties to AAV production. Efficient purification of AAV of several subclasses by affinity chromatography. -
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A02207-40
MonoRabT AAVX VP1 Antibody (24F5), mAb, Rabbit
Price: $666.49List Price: $740.54Adeno-associated virus (AAV) is a single-stranded DNA virus that commonly infects humans without pathology. Therefore, AAV can be engineered to deliver DNA to target cells as a vector for gene therapy. -
A02206-40
MonoRabT AAVX VP1/VP2/VP3 Antibody (5G4), mAb, Rabbit
Price: $666.49List Price: $740.54Adeno-associated virus (AAV) is a single-stranded DNA virus that commonly infects humans without pathology. Therefore, AAV can be engineered to deliver DNA to target cells as a vector for gene therapy.