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advanced detection modes such as Fluorescence Polarization, TimeResolved Fluorescence and Filtered Luminescence (e.g. BRET). A
dual reagent injection system is available to automate inject/read
assays such as ion channels assays or flash luminescence assays (e.g.
luciferase or ATP assays).
To create the ideal environment for live-cell assays, Synergy H1m
offers user-adjustable orbital shaking and advanced 4-Zone
temperature control, plus an available Gas Controller (shown below)
for control and monitoring of CO2 and O2 levels within the Synergy
H1m.
Features:
Specifications:
General
Models:
H1M:
Monochromator-based
Monochromator-based
Filter-based
Hybrid
Optional Accessories:
Typical Applications:
Nucleic acid quantification
Protein quantification
Enzyme kinetics
Biomarker quantification
ELISAs
Genetic analysis
Drug discovery
Cell proliferation
Cytotoxicity
Drug absorption and metabolism
Biologics drug discovery and development
Absorbance
Light source:
Wavelength selection:
Wavelength range:
Bandpass:
Dynamic range:
Resolution:
Pathlength correction:
OD accuracy:
OD repeatability:
Reading speed:
Fluorescence
Intensity
Sensitivity:
Monochromators:
Top: Fluorescein 2.5 pM typical (0.25 fmol/well 384-well
plate)
Bottom: Fluorescein 5 pM typical (0.5 fmol/well 384-well
plate)
Light source:
Xenon flash lamp
Wavelength selection: Double grating monochromators (Top and Bottom)
Wavelength range:
250 700 nm
Dynamic range:
5 decades
Detection system:
PMT
Luminescence
Sensitivity:
Wavelength range:
Monochromator system: 20 amol ATP typical (flash)
300 700 nm
Dynamic range:
>6 decades
Reagent
Dispensers
Dispense precision:
Dispense accuracy:
Number:
Plate geometry:
Dispense volume:
Minimum prime
volume:
<2% at 50 200 L
1 L or 2%
2 syringe pumps
1- to 384-well microplates
5 1000 L in 1 L increment
1 mL, 100 L with back flush
Physical Characteristics
Power:
Dimensions:
Weight:
Food safety
Biofuels research
Environmental monitoring
Hybrid Technolgy is protected under US Patent 8,218,141.
Rev. 12/18/12