Cat# | Name | |||||||||||||
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![]() | 303-INJ | Injectable native Coelenterazine, highly pure (99.7%) and op ... | ![]() Injectable native Coelenterazine, highly pure (99.7%) and optimized for in vivo research.
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Recommended path of injection: intra-peritoneal cavity. For animal use only. | |||||||||||
![]() | 301-INJ | Injectable h-Coelenterazine, highly pure (99%) and optimized ... | ![]() Injectable h-Coelenterazine, highly pure (99%) and optimized for in vivo research.
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Benzyl Coelenterazine (h-CTZ) in sterile injection vials with a low retention volume. Each kit is supplied with two ‘Inject-A-Lume’ vials of 500 µg h-CTZ and a sterile ‘Fuel-Inject’ diluent. For animal use only. | |||||||||||
![]() | 355-INJ | e-CTZ is now available in sterile injection vials with a low ... | ![]() e-CTZ is now available in sterile injection vials with a low retention volume. Each kit is suppled with two ‘Inject-A-Lume’ vials of 500 ug e-CTZ and 500 ul of steril ‘Fuel-Inject’ diluent. It was reported that this analogue enhances the signal by two-fold in Renilla Luciferase in vivo studies.
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e-coelenterazine or Coelenterazine-E (e-CTZ) is a synthetic analogue of native Coelenterazine with an additional ethyl group, forming an additional ring system. First described by Shimomura in 1989. For Renilla muelleri Luciferase, an increase of 750% in initial intensity and 137% in total light was observed using e-Coelenterazine compared to naitve Coelenterazine.
Note: In will not be utilized by Gaussia Luciferase. |