632381/632380/632475/632569/632593/632592/632474/632598-Antibodies to detect GFP, ZsGreen1, AcGFP1, or EGFP- Takara

A monoclonal antibody produced by hybridoma cells against full-length Aequorea victoria green fluorescent protein (GFP). This antibody recognizes native and denatured forms of wild-type GFP, GFPuv, AcGFP, EGFP, destabilized EGFP variants, EBFP, EYFP, ECFP, AcGFP, and both N- and C-terminal fusion proteins containing these GFP variants in bacterial and mammalian cell lysates.

A monoclonal antibody produced by hybridoma cells against full-length Aequorea victoria green fluorescent protein (GFP). This antibody recognizes native and denatured forms of wild-type GFP, GFPuv, AcGFP, EGFP, destabilized EGFP variants, EBFP, EYFP, ECFP, AcGFP, and both N- and C-terminal fusion proteins containing these GFP variants in bacterial and mammalian cell lysates.

Influenza virus is classified into three groups (A, B, and C). Clinically prevalent types of Influenza virus are H1, H3 and B strain. Influenza virus is further classified into subtypes based on variances in Neuraminidase (NA) and Haemagglutinin (HA) that are the surface glycoprotein of the virus. H1N1 subtype and H3N2 subtype are known to cause severe febrile illness. An influenza virus particle consists of a head region and a stem region. The head region has a receptor domain and the stem region contains a region required for fusion between the virus and the target cell. Takara offers several influenza antibodies that are useful for various viral detection and typing methods, as well as neutralization assays. These antibodies are for research use only.

pEF1α-mCherry-N1 is a mammalian expression vector that constitutively expresses a protein of interest fused to the N-terminus of the red fluorescent protein mCherry, even after stable integration of the vector into the host cell genome. Stable, constitutive expression of the fusion protein is driven by the human elongation factor 1 alpha (EF1α) promoter, allowing the monitoring of a variety of cellular processes (such as differentiation in primary or stem cells) without the transgene silencing associated with CMV promoters. The unmodified vector can be used to express mCherry in mammalian cells.