Agilent DNA 12000 Reagents
Agilent TechnologiesThe DNA kits are ideal for automated sizing and quantitation of PCR fragments, restriction digests or fragmented DNA.
The DNA kits are ideal for automated sizing and quantitation of PCR fragments, restriction digests or fragmented DNA.
The DNA kits are ideal for automated sizing and quantitation of PCR fragments, restriction digests or fragmented DNA.
Lambda DASH II vector kits offer traditional genomic cloning of 9−23 Kb fragments. All of our vectors for genomic library construction contain T3 and T7 RNA promoters for rapid gene walking and high-resolution gene mapping.
Lambda DASH II vector kits offer traditional genomic cloning of 9−23 Kb fragments. All of our vectors for genomic library construction contain T3 and T7 RNA promoters for rapid gene walking and high-resolution gene mapping.
The TaqPlus Precision polymerase mixture is an optimized blend of Stratagene cloned Pfu DNA polymerase and Taq2000 DNA polymerase, a highly purified, recombinant version of Taq DNA polymerase. The TaqPlus Precision PCR system exhibits the highest replication accuracy achieved using DNA polymerase mixtures.
Taq Extender PCR additive improves the reliability and yield of conventional Taq-based PCR amplifications. Taq Extender additive increases the efficiency of Taq DNA polymerase extension reactions during each cycle of PCR by reducing mismatch pausing, resulting in a greater percentage of completed extension reactions.
Microalbumin reagents for use as open channel on commercially available chemistry analyzers.
The Follistatin enzyme linked immunosorbent assay (ELISA) kit provides materials for the quantitative measurement of total follistatin (288, 300, 315) in human serum and other biological fluids.
PrimeStore MTM is designed to rapidly inactivate viruses (including Influenza), bacteria (including Mycobacterium tuberculosis, MTB) and veterinary pathogens (ASFv, CSFv, FMDv, HPAI, and NDv) at point-of-collection and stabilize DNA and RNA during storage and shipping.
Streamline the identification of heritable disease-linked alleles, be it through carrier screening or pre- and post-natal testing.
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