Empowering Scientific Discovery

Huazhi Taik Bio-Technologies (Beijing) Co., Ltd.

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BrandASPEC
OriginUSA
ManufacturerIonSense, Inc.
ModelASAP
Instrument TypeAtmospheric Pressure Ionization Source
Mass Range5–3000 amu
Sensitivitypg-level (dependent on coupled mass spectrometer)
ResolutionDetermined by host MS platform
Accurate Mass CapabilityEnabled via compatible high-resolution MS (e.g., Orbitrap, FT-ICR, QTOF)
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BrandASPEC (Prosolia)
OriginUSA
ModelFlowprobe
Instrument TypeAmbient Ion Source
Compatible MS PlatformsThermo Orbitrap, Bruker timsTOF, SCIEX TripleTOF & QTRAP
Sample InterfaceLiquid Microjet Surface Sampling Probe (LMJ-SSP)
Spatial Resolution~630 µm (rapid profiling), down to ~50 µm (high-res DESI-2D integration)
Operating ModeReal-time, continuous-flow in situ microextraction coupled with ESI ionization
Optical GuidanceIntegrated coaxial camera for real-time probe positioning and surface navigation
Application ScopeLabel-free molecular imaging of tissues, single-cell metabolomics, spatially resolved lipidomics/peptidomics, forensic toxicology, dried blood spot (DBS) analysis, time-resolved pharmacokinetics
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BrandASPEC (Huazhi Taike)
OriginGermany
ManufacturerPlasmion GmbH
ModelSICRIT® SC-20X
Dimensions250 × 180 × 80 mm
Weight2.4 kg
Power SupplyStandard 100–240 V AC, 50/60 Hz
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BrandASPEC
OriginUSA
Manufacturer TypeAuthorized Distributor
Origin CategoryImported
ModelNimbus
Instrument TypeElectrospray Ionization (ESI) Source
CompatibilityThermo and SCIEX LC-MS Systems
Operating ModeStandalone (No External PC or Software Required)
Key TechnologyIntegrated eFrit Nanospray Emitters, Dual-Column Switching, On-Chip Column Heating & Temperature Control, Active Spray Tip Purging with Sheath Nitrogen Gas
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BrandAdvion
OriginUSA
ModelTriVersa NanoMate®
Instrument TypeChip-Based Nanoelectrospray Ion Source
Mass Range100 Da – 100 kDa
SensitivityDependent on Coupled Mass Spectrometer
ResolutionDependent on Coupled Mass Spectrometer
Accurate Mass CapabilityDependent on Coupled Mass Spectrometer
ComplianceASTM E2915, ISO/IEC 17025 (when operated in GLP/GMP environments), FDA 21 CFR Part 11–ready software architecture
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