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Routine Reagents for Coagulation Testing
Phosphoplastin RL
Catalogue Number: 11-305Size: 10 x 5 mL (500 tests/kit)
Liquid Thromboplastin Kits ISI <1.3. for Prothrombin Time assays.
Phosphoplastin RL is intended for use in the one-stage Prothrombin Time (PT) test and in PT based hemostasis assays. The PT can be used to screen for coagulopathies, for extrinsic factor assays, and for therapeutic monitoring of Warfarin and related drugs.
The Prothrombin Time (PT) Test is used to:
- Screen for congenital or acquired deficiencies in the extrinsic and common pathways
- Monitor warfarin therapy
- Aid in diagnosis of DIC
- Aid in diagnosis of inhibitors to Factors II, V, and X.
Phosphoplastin RL
Catalogue Number: 11-310Size: 10 x 10 mL (1000 tests/kit)
Liquid Thromboplastin Kit ISI <1.3 for Prothrombin Time assays.
Phosphoplastin RL is intended for use in the one-stage Prothrombin Time (PT) test and in PT based hemostasis assays. The PT can be used to screen for coagulopathies, for extrinsic factor assays, and for therapeutic monitoring of Warfarin and related drugs.
The Prothrombin Time (PT) Test is used to:
- Screen for congenital or acquired deficiencies in the extrinsic and common pathways
- Monitor warfarin therapy
- Aid in diagnosis of DIC
- Aid in diagnosis of inhibitors to Factors II, V, and X.
Phospholin ES
Catalogue Number: 21-405Size: 5 x 5 mL (500 tests/kit)
Ellagic Acid APTT Reagent & 25 mM Calcium Chloride.
Phospholin ES APTT reagent is an ellagic acid based reagent with soybean phospholipids, buffers, stabilizers and preservatives. Phospholin ES is intended for use as an activated partial thromboplastin time (APTT) reagent. The APTT test is a qualitative assay used in routine coagulation screening of patient plasma to detect deficiencies in the intrinsic pathway. It is also used to monitor heparin therapy and in the detection of Lupus Anticoagulants. Phospholin ES is to be used by qualified laboratory personnel.
The APTT Test is used to:
- Screen for congenital or acquired deficiencies in the intrinsic and contact pathways
- Monitor heparin therapy
- Aid in diagnosis of Lupus Anticoagulants
- Aid in diagnosis of inhibitors to Factors VIII, IX, and XI.
Phospholin ES
Catalogue Number: 21-410Size: 10 x 10 mL (1000 tests/kit)
Ellagic Acid APTT Reagent & 25 mM Calcium Chloride.
Phospholin ES APTT reagent is an ellagic acid based reagent with soybean phospholipids, buffers, stabilizers and preservatives. Phospholin ES is intended for use as an activated partial thromboplastin time (APTT) reagent. The APTT test is a qualitative assay used in routine coagulation screening of patient plasma to detect deficiencies in the intrinsic pathway. It is also used to monitor heparin therapy and in the detection of Lupus Anticoagulants. Phospholin ES is to be used by qualified laboratory personnel.
The APTT Test is used to:
- Screen for congenital or acquired deficiencies in the intrinsic and contact pathways
- Monitor heparin therapy
- Aid in diagnosis of Lupus Anticoagulants
- Aid in diagnosis of inhibitors to Factors VIII, IX, and XI.
Plasma Controls and Reference Plasmas
Plasmacon N
Catalogue Number: 30-201Size: 10 x 1 mL (200 tests/kit)
Normal Control Plasma.
PlasmaCon N is a human lyophilized plasma control intended for use as a normal control with citrated plasma to monitor the performance of the Prothrombin Time (PT) and Activated Partial Thromboplastin Time (APTT) tests.
Plasmacon L-1
Catalogue Number: 31-201Size: 10 x 1 mL (200 tests/kit)
Mildly Abnormal Control Plasma.
PlasmaCon L-1 is a human lyophilized plasma control intended for use as a mid-level abnormal control with citrated plasma to monitor the performance of the Prothrombin Time (PT) and Activated Partial Thromboplastin Time (APTT) tests.
Plasmacon L-2
Catalogue Number: 32-201Size: 10 x 1 mL (200 tests/kit)
Highly Abnormal Control Plasma.
PlasmaCon L-2 is a human lyophilized plasma control intended for use as a high level abnormal control with citrated plasma to monitor the performance of the Prothrombin Time (PT) and Activated Partial Thromboplastin Time (APTT) tests.
Plasmacon LA
Catalogue Number: 150-201Size: 10 x 1 mL (200 tests/kit)
LA Positive Control Plasma for LA Reagents.
PlasmaCon LA is intended for use as a LA positive, abnormal quality control plasma to monitor the performance of diagnostic assays, performed in professional clinical laboratories, for the presence of lupus anticoagulants in citrated plasma. PlasmaCon LA is used as an LA positive control plasma for in vitro diagnostic lupus anticoagulant tests in the clinical coagulation laboratory.
Plasmaref ARN
Catalogue Number: 33-201Size: 10 x 1 mL (200 tests/kit)
Assayed Reference Plasma, Normal.
PlasmaRef ARN is an assayed reference normal plasma for use in the quantitative determination of coagulation proteins. PlasmaRef ARN reference plasma is used as plasma calibrators or validators in factor assays.
Plasmaref ARL-2
Catalogue Number: 35-201Size: 10 x 1 mL (200 tests/kit)
Assayed Reference Plasma, Highly Abnormal.
PlasmaRef ARL-2 is an assayed reference abnormal plasma for use in the quantitative determination of coagulation proteins. PlasmaRef ARL-2 reference plasma is used as plasma calibrators or validators in factor assays.
Fib Calibrator
Catalogue Number: 71-201Size: 10 x 1 mL
Fibrinogen Reference Plasma.
FIB Calibrator is intended for use as a normal reference standard for routine fibrinogen quantitation on citrated plasma. FIB Calibrator may be used to generate a standard reference curve for fibrinogen determination or as a quality control check for stored reference curves in daily fibrinogen testing
r2 diagnostics
Emicizumab Calibrator and Controls
Emicizumab Calibrator
Catalogue Number: 151-201-CESize: 5 x 1 mL
Plasma Calibrator (100 ug/mL Emicizumab)
Emicizumab Calibrator is a calibrator intended for use in the calibration of a modified one-stage FVIII activity assay for the determination of active emicizumab concentration from a clot time measurement performed on an automated coagulation analyzer.
Emicizumab Calibrator may be used together with a modified one-stage FVIII assay to generate a calibration curve for emicizumab determination using citrated plasma from patients with haemophilia A being treated with the drug.
Emicizumab Controls
Catalogue Number: 152-401-CESize: 5 x 1 mL
Plasma Controls, Level 1 (25 ug/mL) Level 2 (75 ug/mL)
Emicizumab Controls Level 1 and Level 2 are assayed controls intended for quality control of a modified one-stage FVIII activity assay for determination of active emicizumab concentration from a clot time measurement performed on an automated coagulation analyzer.
Emicizumab Controls may be used together with Emicizumab Calibrator and a modified one-stage FVIII assay as QC material for use in a laboratory's quality control program.
r2 Diagnostics
Immunodepleted Plasmas
NoFact II
Catalogue Number: 62-201Size: 10 x 1 mL (200 tests/kit)
Factor II Depleted Plasma.
The NoFact Deficient Substrate Plasma is intended for the quantitative determination of that Factor in patients suspected of having a congenital or acquired deficiency of this coagulation protein. NoFact II depleted plasma is used in Factor assays of the extrinsic and common pathway using the PT.
NoFact V
Catalogue Number: 65-201Size: 10 x 1 mL (200 tests/kit)
Factor V Depleted Plasma.
The NoFact Deficient Substrate Plasma is intended for the quantitative determination of that Factor in patients suspected of having a congenital or acquired deficiency of this coagulation protein. NoFact V depleted plasma is used in Factor assays of the extrinsic and common pathway using the PT.
NoFact VII
Catalogue Number: 67-201Size: 10 x 1 mL (200 tests/kit)
Factor VII Depleted Plasma.
The NoFact Deficient Substrate Plasma is intended for the quantitative determination of that Factor in patients suspected of having a congenital or acquired deficiency of this coagulation protein. NoFact VII depleted plasma is used in Factor assays of the extrinsic and common pathway using the PT.
NoFact VIII
Catalogue Number: 68-201Size: 10 x 1 mL (200 tests/kit)
Factor VIII Depleted Plasma.
The NoFact Deficient Substrate Plasma is intended for the quantitative determination of that Factor in patients suspected of having a congenital or acquired deficiency of this coagulation protein. NoFact VIII depleted plasma is used in Factor assays of the intrinsic using the APTT.
NoFact IX
Catalogue Number: 69-201Size: 10 x 1 mL (200 tests/kit)
Factor IX Depleted Plasma.
The NoFact Deficient Substrate Plasma is intended for the quantitative determination of that Factor in patients suspected of having a congenital or acquired deficiency of this coagulation protein. NoFact IX depleted plasma is used in Factor assays of the intrinsic using the APTT.
NoFact X
Catalogue Number: 60-201Size: 10 x 1 mL (200 tests/kit)
Factor X Depleted Plasma.
The NoFact Deficient Substrate Plasma is intended for the quantitative determination of that Factor in patients suspected of having a congenital or acquired deficiency of this coagulation protein. NoFact X depleted plasma is used in Factor assays of the extrinsic and common pathway using the PT.
NoFact XI
Catalogue Number: 61-201Size: 10 x 1 mL (200 tests/kit)
Factor XI Depleted Plasma.
The NoFact Deficient Substrate Plasma is intended for the quantitative determination of that Factor in patients suspected of having a congenital or acquired deficiency of this coagulation protein. NoFact XI depleted plasma is used in Factor assays of the intrinsic using the APTT.
NoFact XII
Catalogue Number: 66-201Size: 10 x 1 mL (200 tests/kit)
Factor XII Depleted Plasma.
The NoFact Deficient Substrate Plasma is intended for the quantitative determination of that Factor in patients suspected of having a congenital or acquired deficiency of this coagulation protein. NoFact XII depleted plasma is used in Factor assays of the intrinsic using the APTT.
Thrombophilia Testing
Thrombotek PSe
Catalogue Number: 90-480Size: 80-160 Determinations (80 tests/kit)
Protein S Assay (clotting assay).
ThromboTek PSe is a complete kit for the quantitative determination of Protein S activity in human plasma by clotting assay. ThromboTek PSe is a factor assay for Protein S activity.
Lupus Anticoagulant and Antiphospholipid Syndrome
Lupotek Detectin VL
Catalogue Number: 85-202Size: 10 x 2 mL (200 tests/kit)
Venom Screening Assay for Lupus Anticoagulants.
LupoTek DetecTin VL and CorrecTin VL test kits are qualitative tests intended to aid in the detection of lupus anticoagulants in citrated plasma by the dilute Russell’s viper venom method in professional clinical laboratories. LupoTek Detectin VL and Correctin VL are used in a panel of diagnostic assays to aid in detection of Lupus anticoagulants.
Lupotek Correctin VL
Catalogue Number: 86-201Size: 10 x 1 mL (100 tests/kit)
Venom Confirmatory Assay for Lupus Anticoagulants.
LupoTek DetecTin VL and CorrecTin VL test kits are qualitative tests intended to aid in the detection of lupus anticoagulants (LA) in citrated plasma by the dilute Russell’s viper venom method in professional clinical laboratories. LupoTek Detectin VL and Correctin VL are used in a panel of diagnostic assays to aid in detection of Lupus anticoagulants.
Lupotek KCT
Catalogue Number: 87-305Size: 5 x 5 mL (500 tests/kit)
Screening Assay for Lupus Anticoagulants.
The LupoTek kaolin clotting time (KCT) is a kaolin activated partial thromboplastin reagent without phospholipid. The LupoTek KCT is a qualitative in vitro coagulation screening assay for use in professional laboratories as an aid in the detection of circulating lupus-like anticoagulants in citrated human plasma. LupoTek KCT is used in a panel of diagnostic assays to aid in detection of Lupus anticoagulants.
Fibrinogen Reagents
Fibrotek Fibrinogen Kit
Catalogue Number: 70-410Size: 100-200 Determinations (200 tests/kit)
Fibrinogen Kit (100 NIH units, Thrombin, human; Clauss method).
The Fibrotek Fibrinogen Kit is intended for use in the quantitative determination of fibrinogen in citrated human plasma. FibroTek Fibrinogen kit is a complete kit for the Clauss determination of fibrinogen, useful in the diagnosis of DIC, liver failure, qualitative abnormalities of fibrinogen, or quantitative deficiency of fibrinogen.
T-Tek
Catalogue Number: 50-201Size: 10 x 1 mL (100 tests/kit)
Thrombin Time reagent (7.5 NIH units, human).
The T-Tek thrombin time reagent is intended for use in the quantitative determination of Thrombin Time (TT) in citrated human plasma in the general patient population. T-Tek should be used in the clinical laboratory by qualified laboratory professionals. The test may be performed using manual methods or semi-automated or automated coagulation analyzers.
Solutions
Calcium Chloride
Catalogue Number: 40-305Size: 10 x 5 mL (1000 tests/kit)
0.025 M Calcium Chloride. Suitable as an initiating reagent for APTT based assays.
Calcium Chloride
Catalogue Number: 40-310Size: 10 x 10 mL (2000 tests/kit)
0.025 M Calcium Chloride. Suitable as an initiating reagent for APTT based assays.