For the quantitative determination of Estrone in human saliva by a chemiluminesc
For the quantitative determination of Estrone in human saliva by a chemiluminescence immunoassay.
The Quantitative Determination of Free Thyroxine Concentration in Human Serum or
The Quantitative Determination of Free Thyroxine Concentration in Human Serum or Plasma by a Microplate Enzyme Immunoassay.
The Leptospira IgG ELISA test is an enzyme immunoassay for the detection of anti
The Leptospira IgG ELISA test is an enzyme immunoassay for the detection of antibodies to Leptospira biflexa (serovar patoc 1) for the serological confirmation of infections in serum and plasma.
The Quantitative Determination of Free Thyroxine Concentration in Human Serum or
The Quantitative Determination of Free Thyroxine Concentration in Human Serum or Plasma by a Microplate Enzyme Immunoassay.
KLI
Enzyme immunoassay, non-radiolabeled, total thyroxine
The Quantitative Determination of Luteinizing Hormone Concentration in Human Ser
The Quantitative Determination of Luteinizing Hormone Concentration in Human Serum by a Microplate Enzyme Immunoassay, Colorimetric.
For the Quantitative Determination of Follicle Stimulating Hormone Concentration
For the Quantitative Determination of Follicle Stimulating Hormone Concentration in Human Serum by a Microplate Enzyme Immunoassay, Colorimetric.
The DRG ACTH ELISA is intended for the quantitative determination of ACTH (Adren
The DRG ACTH ELISA is intended for the quantitative determination of ACTH (Adreno-corticotropic Hormone) in human plasma.
The Toxocara ELISA test is a semi-quantitative enzyme immunoassay for the detect
The Toxocara ELISA test is a semi-quantitative enzyme immunoassay for the detection of antibodies to Toxocara, in samples of human serum or plasma.
For the qualitative determination of serum or plasma antibodies in humans, prima
For the qualitative determination of serum or plasma antibodies in humans, primarily IgG, to Schistosoma spp. using the ELISA technique.
For the direct quantitative determination of Pregnenolone by an enzyme immunoass
For the direct quantitative determination of Pregnenolone by an enzyme immunoassay in human serum.
The EPO ELISA is intended for the quantitative determination of Erythropoietin (
The EPO ELISA is intended for the quantitative determination of Erythropoietin (EPO) in human serum.
The DRG Candida albicans IgG Enzyme Immunoassay Kit provides materials for the q
The DRG Candida albicans IgG Enzyme Immunoassay Kit provides materials for the qualitative andsemiquantitative determination of IgG-class antibodies to Candida albicans in serum.
For the quantitative determination of thyroid stimulating hormone (TSH) concentr
For the quantitative determination of thyroid stimulating hormone (TSH) concentration in human serum. The assay is useful in the diagnosis of thyroid or pituitary disorders.
Micro-Albumin ELISA is a competitive test system for the quantitative measuremen
Micro-Albumin ELISA is a competitive test system for the quantitative measurement of human albumin in urine.
JIR
INDICATOR METHOD, PROTEIN OR ALBUMIN (URINARY, NON-QUANT.)
This is a test for the qualitative detection of human Chorionic Gonadotropin (HC
This is a test for the qualitative detection of human Chorionic Gonadotropin (HCG) in urine.
The hCG ELISA is intended for the quantitative determination of human chorionic
The hCG ELISA is intended for the quantitative determination of human chorionic gonadotropin (hCG) concentration in human serum. The assay is for use in the early diagnosis of pregnancy in a clinical laboratory setting.
The DRG neonatal Galactose ELISA is designed for the quantitative determination
The DRG neonatal Galactose ELISA is designed for the quantitative determination of galactose in neonatal blood spots. It is for in vitro diagnostic use as an aid in screening newborns for elevated galactose levels as seen in galactosemia.
The DRG Galactose kit is designed for the quantitative determination of galactos
The DRG Galactose kit is designed for the quantitative determination of galactose in neonatal blood spots. It is for in-vitro diagnostic use as an aid in screening newborns for the elevated galactose levels as seen in galactosemia.
The Quantitative Determination of Free Triiodothyronine Concentration in Human S
The Quantitative Determination of Free Triiodothyronine Concentration in Human Serum by a Microplate Enzyme Immunoassay.
For the direct quantitative determination of Pregnenolone by enzyme immunoassay
For the direct quantitative determination of Pregnenolone by enzyme immunoassay in human serum.
The Quantitative Determination of Free Triiodothyronine Concentration in Human S
The Quantitative Determination of Free Triiodothyronine Concentration in Human Serum by a Microplate Enzyme Immunoassay.
The Adenovirus Stool Antigen Detection ELISA is an in vitro procedure for the qu
The Adenovirus Stool Antigen Detection ELISA is an in vitro procedure for the qualitative determination of adenovirus antigen in feces.IVD Research
This is a test for the qualitative detection of human Chorionic Gonadotropin (HC
This is a test for the qualitative detection of human Chorionic Gonadotropin (HCG) in urine.
The DRG Rheumatoid Factor (RF) IgM ELISA test system is intended for the qualita
The DRG Rheumatoid Factor (RF) IgM ELISA test system is intended for the qualitative and semi-quantitative detection of RF IgM-class antibody in human sera. The test system is intended to be used as an aid in the diagnosis of rheumatoid arthritis.
The Beta-2 Microglobulin ELISA is intended for the quantitative determination of
The Beta-2 Microglobulin ELISA is intended for the quantitative determination of ß2-microglobulin in human serum.
The DRG neonatal Galactose ELISA is designed for the quantitative determination
The DRG neonatal Galactose ELISA is designed for the quantitative determination of galactose in neonatal blood spots. It is for in vitro diagnostic use as an aid in screening newborns for elevated galactose levels as seen in galactosemia.
The Quantitative Determination of Thyroglobulin (Tg) Autoantibodies in Human Ser
The Quantitative Determination of Thyroglobulin (Tg) Autoantibodies in Human Serum or Plasma by a Microplate Enzyme Immunoassay, Colorimetric. Measurements of Tg autoantibodies may aid in the diagnosis of certain thyroid diseases such as Hashimoto’s and Grave’s as well as nontoxic goiter.
The Trichinella spiralis IgG ELISA test is a qualitative enzyme immunoassay for
The Trichinella spiralis IgG ELISA test is a qualitative enzyme immunoassay for the detection of antibodies to Trichinella, in samples of human serum or plasma. This test is intended to be performed by trained medical technologists only.
The E. histolytica ELISA test is a qualitative enzyme immunoassay for the detect
The E. histolytica ELISA test is a qualitative enzyme immunoassay for the detection of antibodies to E. histolytica, in samples of human serum or plasma.
KHW
ANTIGEN, ID, HA, CEP, ENTAMOEBA HISTOLYTICA & REL. SPP.
The HGH ELISA is intended for the quantitative determination of human growth hor
The HGH ELISA is intended for the quantitative determination of human growth hormone (HGH) concentration in human serum.
This Triiodothyronine (T3) ELISA is intended for the quantitative determination
This Triiodothyronine (T3) ELISA is intended for the quantitative determination of triiodothyronine (T3) concentration inhuman serum. This test is useful in the diagnosis and treatment of thyroid diseases such as hyperthyroidism.
The device is an Enzyme Immunoassay (EIA) for the quantitative measurement of fr
The device is an Enzyme Immunoassay (EIA) for the quantitative measurement of free testosterone in human serum. s and adrogenital syndromes.
CDZ
RADIOIMMUNOASSAY, TESTOSTERONES AND DIHYDROTESTOSTERONE
The Cotinine direct (Serum/Urine) ELISA is a specific and sensitive in-vitro tes
The Cotinine direct (Serum/Urine) ELISA is a specific and sensitive in-vitro test to detect the presence of Cotinine in serum and urine.
The Spotted Fever Group Rickettsia IgG ELISA is intended for the detection of hu
The Spotted Fever Group Rickettsia IgG ELISA is intended for the detection of human IgG class antibody to Spotted Fever Group Rickettsia, to be used as an aid in the diagnosis of human infection by these pathogens.
For the direct quantitative determination of DHEAS by an enzyme immunoassay in h
For the direct quantitative determination of DHEAS by an enzyme immunoassay in human serum.
JKC
RADIOIMMUNOASSAY, DEHYDROEPIANDROSTERONE (FREE AND SULFATE)
For the direct quantitative determination of Free Testosterone by enzyme immunoa
For the direct quantitative determination of Free Testosterone by enzyme immunoassay in human serum. For in vitro diagnostic use only.
CDZ
RADIOIMMUNOASSAY, TESTOSTERONES AND DIHYDROTESTOSTERONE
The Strongyloides ELISA test is a qualitative enzyme immunoassay for the detecti
The Strongyloides ELISA test is a qualitative enzyme immunoassay for the detection of antibodies to Strongyloides, in samples of human serum or plasma.
The Quantitative Determination of Thyroid Peroxidase (TPO) Autoantibodies in Hum
The Quantitative Determination of Thyroid Peroxidase (TPO) Autoantibodies in Human Serum or Plasma by a Microplate Enzyme Immunoassay. Measurements of TPO autoantibodies may aid in the diagnosis of certain thyroid diseases such as Hashimoto’s and Grave’s as well as nontoxic goiter.
The Myoglobin ELISA is intended for the quantitative determination of myoglobin
The Myoglobin ELISA is intended for the quantitative determination of myoglobin in human serum.
The C-Reactive Protein HS ELISA is intended for the quantitative determination o
The C-Reactive Protein HS ELISA is intended for the quantitative determination of C-reactive protein (CRP) in human serum.Enhanced sensitivity measurements of CRP can be useful for the detection and evaluation of infection, tissue injury, inflammatory disorders and associated diseases.
DCK
C-REACTIVE PROTEIN, ANTIGEN, ANTISERUM, AND CONTROL
The Mumps Virus IgG ELISA is intended for the qualitative determination of IgG c
The Mumps Virus IgG ELISA is intended for the qualitative determination of IgG class antibodies against Mumps Virus in human serum or plasma (citrate, heparin).
The Measles Virus IgG ELISA is intended for the qualitative determination of IgG
The Measles Virus IgG ELISA is intended for the qualitative determination of IgG class antibodies against Measles Virus in human serum or plasma (citrate, heparin).
The Prolactin ELISA is intended for the quantitative determination of prolactin
The Prolactin ELISA is intended for the quantitative determination of prolactin in human serum. The assay is useful in the diagnosis and treatment of disorders of the anterior pituitary and hypothalamus.
For the quantitative determination of total thyroxine (T4) concentration in huma
For the quantitative determination of total thyroxine (T4) concentration in human serum. The test is useful in the diagnosis and treatment of thyroid disorders.
KLI
Enzyme immunoassay, non-radiolabeled, total thyroxine
For the qualitative screening of serum or plasma IgG antibodies to Ascaris using
For the qualitative screening of serum or plasma IgG antibodies to Ascaris using an Enzyme Linked Immunoabsorbant Assay (ELISA) technique.
The Calcitonin ELISA is intended for the quantitative determination of Calcitoni
The Calcitonin ELISA is intended for the quantitative determination of Calcitonin in human serum.
The PTH (Parathyroid) Intact ELISA is intended for the quantitative determinatio
The PTH (Parathyroid) Intact ELISA is intended for the quantitative determination of Intact-PTH (Parathyroid Hormone) in human serum.
For the qualitative screening of serum or plasma IgG antibodies to Taenia solium
For the qualitative screening of serum or plasma IgG antibodies to Taenia solium using an Enzyme Linked Immunoabsorbant Assay (ELISA) technique.NLD
The Total IgE ELISA is intended for use in the quantitative determination of imm
The Total IgE ELISA is intended for use in the quantitative determination of immunoglobulin E in human serum. The assay is to be used for the assessment of hypersensitive and allergic reactions in patients.
The Access Total IgE assay is a paramagnetic particle, chemiluminescent immunoas
The Access Total IgE assay is a paramagnetic particle, chemiluminescent immunoassay for the qualitative determination of total E (IgE) levels in human serum and plasma (heparin, EDTA) using the Access Immunoassay Systems.
The Access Total IgE Calibrators are intended to calibrate the Access Total IgE
The Access Total IgE Calibrators are intended to calibrate the Access Total IgE assay for the quantitative determination of total IgE levels in human serum and plasma (heparin, EDTA) using the Access Immunoassay Systems.
The Access Total IgE Calibrator S0 is intended for use with the Access Total IgE
The Access Total IgE Calibrator S0 is intended for use with the Access Total IgE assay to dilute patient samples containing analyte concentrations greater than the analyte specific S6 calibrator.
Contains one bottle of Total IgE Conjugate and four vials of each Total IgE Curv
Contains one bottle of Total IgE Conjugate and four vials of each Total IgE Curve Control (CC-1, CC-2) for the ImmunoCAP Total IgE method.
Contains three vials of each Total IgE Curve Control (CC-1, CC-2) for the Immuno
Contains three vials of each Total IgE Curve Control (CC-1, CC-2) for the ImmunoCAP Total IgE method.
Contains one vial of each Total IgE Calibrator (Cal-2, Cal-10, Cal-50, Cal-200,
Contains one vial of each Total IgE Calibrator (Cal-2, Cal-10, Cal-50, Cal-200, Cal-1000, Cal-5000) to form a complete calibration curve for the ImmunoCAP Total IgE method.
An IgE test system is a device intended for the quantitative in vitro determinat
An IgE test system is a device intended for the quantitative in vitro determination of immunoglobulin E (IgE) concentration in human serum or plasma
This product is intended for in vitro diagnostic use in the quality control of I
This product is intended for in vitro diagnostic use in the quality control of IgE on clinical chemistry systems.
BioCheck IgE EIA Test Kit is intended for the quantitative determination of immu
BioCheck IgE EIA Test Kit is intended for the quantitative determination of immunoglobulin E (IgE) in human serum.
For the quantitative measurement of immunoglobulin E in human serum and plasma (
For the quantitative measurement of immunoglobulin E in human serum and plasma (heparin or EDTA) on the Dimension Vista® System
DImension Vista® Immunoglobulin E Flex® reagent cartridge
The DRG IgE ELISA is intended for the quantitative determination of immunoglobul
The DRG IgE ELISA is intended for the quantitative determination of immunoglobulin E in human serum. This assay is to be used for the assessment of hypersensitive and allergic reactions in patients.
A substance or reactant intended to be used together with a parent IVD to perfor
A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of an allergen specific immunoglobulin E (IgE) antibody in a clinical specimen.
A substance or reactant intended to be used together with a parent IVD to perfor
A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of an allergen specific immunoglobulin E (IgE) antibody in a clinical specimen.
A substance or reactant intended to be used together with a parent IVD to perfor
A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of an allergen specific immunoglobulin E (IgE) antibody in a clinical specimen.
A substance or reactant intended to be used together with a parent IVD to perfor
A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of an allergen specific immunoglobulin E (IgE) antibody in a clinical specimen.
A substance or reactant intended to be used together with a parent IVD to perfor
A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of an allergen specific immunoglobulin E (IgE) antibody in a clinical specimen.
A substance or reactant intended to be used together with a parent IVD to perfor
A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of an allergen specific immunoglobulin E (IgE) antibody in a clinical specimen.
A substance or reactant intended to be used together with a parent IVD to perfor
A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of an allergen specific immunoglobulin E (IgE) antibody in a clinical specimen.
A substance or reactant intended to be used together with a parent IVD to perfor
A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of an allergen specific immunoglobulin E (IgE) antibody in a clinical specimen.
A substance or reactant intended to be used together with a parent IVD to perfor
A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of an allergen specific immunoglobulin E (IgE) antibody in a clinical specimen.
A substance or reactant intended to be used together with a parent IVD to perfor
A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of an allergen specific immunoglobulin E (IgE) antibody in a clinical specimen.
A substance or reactant intended to be used together with a parent IVD to perfor
A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of an allergen specific immunoglobulin E (IgE) antibody in a clinical specimen.
A substance or reactant intended to be used together with a parent IVD to perfor
A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of an allergen specific immunoglobulin E (IgE) antibody in a clinical specimen.
A substance or reactant intended to be used together with a parent IVD to perfor
A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of an allergen specific immunoglobulin E (IgE) antibody in a clinical specimen.
A substance or reactant intended to be used together with a parent IVD to perfor
A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of an allergen specific immunoglobulin E (IgE) antibody in a clinical specimen.
A substance or reactant intended to be used together with a parent IVD to perfor
A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of an allergen specific immunoglobulin E (IgE) antibody in a clinical specimen.
A substance or reactant intended to be used together with a parent IVD to perfor
A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of an allergen specific immunoglobulin E (IgE) antibody in a clinical specimen.
A substance or reactant intended to be used together with a parent IVD to perfor
A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of an allergen specific immunoglobulin E (IgE) antibody in a clinical specimen.
A substance or reactant intended to be used together with a parent IVD to perfor
A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of an allergen specific immunoglobulin E (IgE) antibody in a clinical specimen.
A substance or reactant intended to be used together with a parent IVD to perfor
A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of an allergen specific immunoglobulin E (IgE) antibody in a clinical specimen.