Hyphen BioMed
GFC Control Plasmas
The GFC Control Plasmas kit is a set of control plasmas lyophilized intended for the quality control of the kit GFC-Test in plasma.
PT Calibrator Set
PT Calibrator Set is a set of five certified plasmas for PT/INR and PT% calibration and/or for verification of local ISI test system. This kit is for research use only and must not be used for patient diagnosis or treatment.
LA Control Plasma High
In US: For Research Use Only. Not for Use in Diagnostic Procedures. LA Control Plasma High Kit is a set of lyophilized quality control plasmas, high positive, for use in Lupus Anticoagulant in vitro clotting assays. This kit is optimized for being used with the HEMOCLOT LA-S and HEMOCLOT LA-C assays.
LA Control Plasma High
For In Vitro Diagnostic Use. In EU: This Product is CE Marked. Health Canada Licensed. LA Control Plasma High Kit is a set of lyophilized quality control plasmas, high positive, for use in Lupus Anticoagulant in vitro clotting assays. This kit is optimized for being used with the HEMOCLOT LA-S and HEMOCLOT LA-C assays.
LA Control Plasma Weak
In US: For Research Use Only. Not for Use in Diagnostic Procedures. LA Control Plasma Weak Kit is a set of lyophilized quality control plasmas, weak positive, for use in Lupus Anticoagulant in vitro clotting assays. This kit is optimized for being used with the HEMOCLOT LA-S and HEMOCLOT LA-C assays.
LA Control Plasma Weak
For In Vitro Diagnostic Use. In EU: This Product is CE Marked. Health Canada Licensed. LA Control Plasma Weak Kit is a set of lyophilized quality control plasmas, weak positive, for use in Lupus Anticoagulant in vitro clotting assays. This kit is optimized for being used with the HEMOCLOT LA-S and HEMOCLOT LA-C assays .
LA Control Plasma
In US: For Research Use Only. Not for Use in Diagnostic Procedures. LA Positive Control Plasma Kit is a set of lyophilized quality control plasmas, weak and high positive, for use in Lupus Anticoagulants in vitro clotting assays. This kit is optimized for being used the HEMOCLOT LA-S and HEMOCLOT LA-C Assays.
LA Control Plasma
For In Vitro Diagnostic Use. In EU: This Product is CE Marked. Health Canada Licensed. LA Positive Control Plasma Kit is a set of lyophilized quality control plasmas, weak and high positive, for use in Lupus Anticoagulants in vitro clotting assays. This kit is optimized for being used the HEMOCLOT LA-S and HEMOCLOT LA-C Assays .
Argatroban Control Plasma
In US: For Research Use Only. Not for Use in Diagnostic Procedures. Set of control plasmas for the quality control of Argatroban (also called Argatra, Arganova or Novastan) measurements, using anti-IIa clotting assays. This kit is optimized for being used with the HEMOCLOT Thrombin Inhibitors assay (low range protocol) .
Argatroban Control Plasma
For In Vitro Diagnostic Use. In EU: This Product is CE Marked. Health Canada Licensed. Set of control plasmas for the quality control of Argatroban (also called Argatra, Arganova or Novastan) measurements, using anti-IIa clotting assays. This kit is optimized for being used with the HEMOCLOT Thrombin Inhibitors assay (low range protocol).
Argatroban Plasma Calibrator
In US: For Research Use Only. Not for Use in Diagnostic Procedures. Set of calibration plasmas for Argatroban (also called Argatra, Arganova, or Novastan), measurements, titrated and optimized using the anti-IIa clotting assay HEMOCLOT Thrombin Inhibitors .
Argatroban Plasma Calibrator
For In Vitro Diagnostic Use. In EU: This Product is CE Marked. Health Canada Licensed. Set of calibration plasmas for Argatroban (also called Argatra, Arganova, or Novastan), measurements, titrated and optimized using the anti-IIa clotting assay HEMOCLOT Thrombin Inhibitors.
ZYMUTESTâ„¢ Total Tissue Factor
For Research Use Only. Not for Use in Diagnostic Procedures. Two-site, enhanced, immuno-assay for measuring human total Tissue Factor (TF), in plasma and purified milieu, or in any biological fluid where TF can be present. This is an ON-DEMAND item which requires minimum order quantity and extended lead time. Please Contact Us for a quote.
ZYMUTESTâ„¢ HIA MonoStrip IgG
In EU: This Product is CE Marked. Health Canada Licensed. Enzyme Immuno-assay designed for measuring heparin-dependent antibodies of the IgG isotype, in human plasma or serum, or in any biological fluid where these antibodies must be measured. This assay measures only the IgG isotype, reported as the most associated with the clinical complications of heparin dependent antibodies (HIT/HITT), allowing confirmation of the diagnosis of HIT/HITT or its clinical suspicion. However, some cases associated with only IgM and/or IgA isotypes can be missed. This kit allows individual test as it offers a packaging for 4 individual 8 well strips along with controls.
ZYMUTESTâ„¢ HIA MonoStrip IgG
In US: 510(k) Cleared for In Vitro Diagnostic Use for Plasma only. Enzyme Immuno-assay designed for measuring heparin-dependent antibodies of the IgG isotype, in human plasma. This assay measures only the IgG isotype, reported as the most associated with the clinical complications of heparin dependent antibodies (HIT/HITT), allowing confirmation of the diagnosis of HIT/HITT or its clinical suspicion. However, some cases associated with only IgM and/or IgA isotypes can be missed. This kit allows individual test as it offers a packaging for 4 individual 8 well strips along with controls.
ZYMUTESTâ„¢ HIA IgGAM
In EU: This Product is CE Marked. Health Canada Licensed. Enzyme immuno-assay designed for measuring globally all heparin-dependent antibodies, whether the isotype is: IgG, IgM and IgA, in human plasma or serum, or in any biological fluid where these antibodies must be measured. This assay is proposed as screening, as an early identification of heparin treated patients presenting a risk to develop HIT or HITT. This assay measures the whole of antibodies. It offers the highest sensitivity as all isotypes are detected. It is the preferred assay when an early detection of heparin dependent antibodies is required for assessing the development risk of HIT/HITT.
ZYMUTESTâ„¢ HIA IgGAM
In US: 510(k) Cleared for In Vitro Diagnostic Use for Plasma only. Enzyme immuno-assay designed for measuring globally all heparin-dependent antibodies, whether the isotype is: IgG, IgM and IgA, in human plasma. This assay is proposed as screening, as an early identification of heparin treated patients presenting a risk to develop HIT or HITT. This assay measures the whole of antibodies. It offers the highest sensitivity as all isotypes are detected. It is the preferred assay when an early detection of heparin dependent antibodies is required for assessing the development risk of HIT/HITT.
ZYMUTESTâ„¢ HIA IgG
In EU: This Product is CE Marked. Health Canada Licensed. Enzyme Immuno-assay designed for measuring heparin-dependent antibodies of the IgG isotype, in human plasma or serum, or in any biological fluid where these antibodies must be measured. This assay measures only the IgG isotype, reported as the most associated with the clinical complications of heparin dependent antibodies (HIT/HITT), allowing confirmation of the diagnosis of HIT/HITT or its clinical suspicion. However, some cases associated with only IgM and/or IgA isotypes can be missed.
ZYMUTESTâ„¢ HIA IgG
In US: 510(k) Cleared for In Vitro Diagnostic Use for Plasma only. Enzyme Immuno-assay designed for measuring heparin-dependent antibodies of the IgG isotype, in human plasma. This assay measures only the IgG isotype, reported as the most associated with the clinical complications of heparin dependent antibodies (HIT/HITT), allowing confirmation of the diagnosis of HIT/HITT or its clinical suspicion. However, some cases associated with only IgM and/or IgA isotypes can be missed.
ZYMUTESTâ„¢ Anti FVIII IgG Mono Strip (IgG-Isotype)
In US and Canada: For Research Use Only. Not for Use in Diagnostic Procedures. The ZYMUTEST Anti-VIII MonoStrip IgG kit is a qualitative or quantitative assay of ELISA sandwich type for measuring auto and allo-antibodies to Factor VIII, of the IgG isotype, in human plasma where auto-antibodies to FVIII must be sought. This kit is for research use only and must not be used to patient diagnosis or treatment. This is an ON-DEMAND item which requires minimum order quantity and extended lead time. Please Contact Us for a quote.
ZYMUTESTâ„¢ vWF:CBA
In US: For Research Use Only. Not for Use in Diagnostic Procedures. The ZYMUTEST vWF:CBA kit is an enzyme-immuno-assay for measuring Collagen Binding Activity (CBA) of human von Willebrand Factor (vWF) in plasma, or in any fluid where this activity needs to be measured.
ZYMUTESTâ„¢ (ACTIVATABLE) TAFI
For Research Use Only. Not for Use in Diagnostic Procedures. Two-site ELISA method, designed with a pair of specific and complementary monoclonal antibodies, for measuring human TAFI zymogen (Thrombin Activatable Fibrinolysis Inhibitor), in plasma, or in any fluid where TAFI can be present. Formerly called “ZYMUTEST proTAFI”. This is an ON-DEMAND item which requires minimum order quantity and extended lead time. Please Contact Us for a quote.
ZYMUTESTâ„¢ Factor VII
For Research Use Only. Not for Use in Diagnostic Procedures. Two-site immuno-assay for measuring human Factor VII (FVII) Antigen in plasma, or in any fluid where FVII can be present. Assay designed with a rabbit polyclonal antibody specific for FVII for coating the ELISA plate and preparation of horse radish peroxidase (HRP).
ZYMUTESTâ„¢ Tissue Factor (Full Length)
For Research Use Only. Not for Use in Diagnostic Procedures. Two-site ELISA method for the measurement of full length Tissue Factor (TF, full length) in human plasma or purified milieu. The kit uses a biotin-streptavidin-HRP system to enhance greatly the sensitivity, thus permitting to detect TF concentration as low as 50 pg/mL. This is an ON-DEMAND item which requires minimum order quantity and extended lead time. Please Contact Us for a quote.
ZYMUTESTâ„¢ Factor X
For Research Use Only. Not for Use in Diagnostic Procedures. Two-site ELISA method for the measurement of coagulation Factor X, in human citrated plasma. Assay designed with affinity purified rabbit polyclonal antibodies for coating the ELISA plate and preparation of Horse Radish Peroxidase (HRP) marker.
ZYMUTESTâ„¢ Factor IX
For Research Use Only. Not for Use in Diagnostic Procedures. Two-site ELISA method for the measurement of coagulation Factor IX, in human citrated plasma. Assay designed with affinity purified rabbit polyclonal antibodies for coating the ELISA plate and preparation of Horse Radish Peroxidase (HRP) marker.
ZYMUTESTâ„¢ Protein Z
For Research Use Only. Not for Use in Diagnostic Procedures. Two-site ELISA method for the measurement of coagulation Protein Z, in human citrated plasma. Assay designed with affinity purified rabbit polyclonal antibodies for coating the ELISA plate and preparation of Horse Radish Peroxidase (HRP) marker.
ZYMUTESTâ„¢ vWF
In US and Canada: For Research Use Only. Not for Use in Diagnostic Procedures. The ZYMUTEST vWF kit is an enzyme-immuno-assay for measuring human von Willebrand Factor (vWF) in plasma, or in any fluid where vWF can be present. Complete ELISA Kit for measuring von Willebrand Factor.
ZYMUTESTâ„¢ Protein C
In US: For Research Use Only. Not for Use in Diagnostic Procedures. Two-site ELISA method for the measurement of coagulation Protein C, in human citrated plasma. Assay designed with affinity purified rabbit polyclonal antibodies for coating the ELISA plate and preparation of Horse Radish Peroxidase (HRP) marker.
ZYMUTESTâ„¢ Protein C
For In Vitro Diagnostic Use. In EU: This Product is CE Marked. Health Canada Licensed. Two-site ELISA method for the measurement of coagulation Protein C, in human citrated plasma. Assay designed with affinity purified rabbit polyclonal antibodies for coating the ELISA plate and preparation of Horse Radish Peroxidase (HRP) marker.
