PerkinElmer

Newborn Screening Reagents

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Use the highest quality reagents available today to screen for core newborn disorders as well as those detected by expanded screening. Our reagents are the industry standard for analytical performance and reliability in detecting congenital diseases that are treatable only when identified during the first days of life.

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Detection Method
  • DELFIA (9)
  • Enzymatic (4)
Disorders
  • Biotinidase (BTD) Deficiency (3)
  • Congenital Adrenal Hyperplasia (CAH) (4)
  • Congenital Hypothyroidism (6)
  • Cystic Fibrosis (4)
  • Galactosemia (5)
  • Glucose-6-phosphate Dehydrogenase (G6PD) Deficiency (2)
  • Hemoglobinopathies (4)
  • Metabolic Disorders (10)
  • Phenylketonuria (2)
  • SCID (3)
Product Brand Name
  • GSP® (9)
  • NeoBase™ (4)
Sample Type
  • Dried blood spots (15)

"Newborn Screening Reagents" 1-43 of 43 Products and Services

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DELFIA® Neonatal Thyroxine (T4) kit (10 plate)

This kit is intended for the quantitative determination of human thyroxine (T4) in blood specimens dried on filter paper as an aid in screening newborns for congenital (neonatal) hypothyroidism.
PerkinElmer

Neonatal GALT kit (10 plate

Neonatal Galactose Transferase (GALT) kits are intended for the semi-quantitative determination of galactose-1-phosphate uridyltransferase (GALT) activity in blood specimens collected onto filter paper, in screening newborns for galactosemia.
EnLite 223

EnLite Neonatal TREC kit, 4 x 96 reactions

The PerkinElmer EnLite Neonatal TREC kit, 4 x 96 reactions (outside USA) is a CE-marked product used with the VICTOR EnLite instrument for the quantitative determination of TREC (T-cell receptor excision circle) DNA in blood specimens dried on a filter paper.
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Neonatal Total Galactose kit (10 plate)

Neonatal Total Galactose kit is intended for the quantitative determination of total galactose (galactose and galactose-1-phosphate) concentrations in blood specimens dried on filter paper as an aid in screening newborns for galactosemia.
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GSP Neonatal Phenylalanine kit

Phenylketonuria (PKU) is a disorder of amino acid metabolism with reported incidence ranging from 1 in 19,000 to 1 in 13,500 newborn infants*. It is caused by an inability to convert phenylalanine to tyrosine due to deficient activity of the enzyme, phenylalanine hydroxylase.
EnLite 223

EnLite Neonatal TREC kit, 1 x 384 reactions

The PerkinElmer EnLite Neonatal TREC kit, 1 x 384 reactions is a CE-marked product used with the VICTOR EnLite instrument for the quantitative determination of TREC (T-cell receptor excision circle) DNA in blood specimens dried on a filter paper.
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Neonatal Phenylalanine kit (10 plate)

Neonatal Phenylalanine kits are intended for the quantitative determination of phenylalanine in blood specimens dried on filter paper as an aid in identifying phenylketonuria in newborns.
EnLite 223

EnLite Neonatal TREC kit, 3 x 384 reactions

EnLite Neonatal TREC is a duplex assay that detects TREC, the marker of SCID, and beta-actin, which is used as an internal control for each specimen.
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MSMS Vitamin D Tool Box

The MSMS Vitamin D Tool Box is intended for in vitro diagnostic use with the MSMS Vitamin D Kit (3075-0010). Product not available in the USA.
GSP Neonatal G6PD kit 3310-0010
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GSP Neonatal GALT kit

Galactosemia is an inherited disorder caused by a deficiency of one of three enzymes responsible for the metabolism of α-D-galactose. The most common form of the disease, classic galactosemia is caused by deficiency of galactose-1-phosphate uridyltransferase (GALT).
PerkinElmer

extendSURE HbFASC Controls

The Haemoglobin FASC control is intended to be used as a position marker monitor for haemoglobin variant analysis methods and to assess assay reproducibility in the following assay types: ion exchange HPLC, capillary electrophoresis, cellulose acetate and agar/agarose gel electrophoresis and iso-electric focusing.
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Neonatal GALT kit (50 plate)

Neonatal Galactose Transferase (GALT) kits are intended for the semi-quantitative determination of galactose-1-phosphate uridyltransferase (GALT) activity in blood specimens collected onto filter paper, in screening newborns for galactosemia.
PerkinElmer

Resolve Hemoglobin kit (135 tests)

The RESOLVE® Systems Hemoglobin Kit use isoelectric focusing (IEF) to detect hemoglobin variants in whole blood, cord blood or blood spot samples.
PerkinElmer

Resolve Hemoglobin kit (3600 tests)

The Wallac RESOLVE® Neonatal Hemoglobin test kit is designed to separate whole blood, cord blood or dried blood spot specimens for detection of normal and variant hemoglobins by isoelectric focusing.
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CHS MSMS Steroids Tool Box

CHS MSMS Steroids Tool Box
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GSP Neonatal Biotinidase kit

GSP Neonatal Biotinidase kit
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GSP Neonatal Thyroxine (T4) kit

Congenital hypothyroidism (CH) results from a failure of the thyroid glands to produce thyroid hormones in adequate amounts. The condition can easily be treated with daily doses of thyroid hormones but clinical diagnosis is difficult to establish and the disease may continue unrecognized for a long time causing irreversible brain damage.
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AutoDELFIA Neonatal 17α-OHP kit (12 plate)

This kit is intended for the quantitative determination of human 17-OH-progesterone in blood specimens dried on filter paper as an aid in screening newborns for congenital adrenal hyperplasia (CAH) using the 1235 AutoDELFIA® automatic immunoassay system.
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GSP Neonatal 17α-OH-progesterone kit

Congenital adrenal hyperplasia (CAH) is a genetic disorder and the most severe form of the disease can lead to a life threatening condition during the first weeks of life. The disease is caused by enzyme defects in steroid biosynthesis, the most frequent types being 21- and 11α-hydroxylase deficiency.
PerkinElmer

Neonatal Biotinidase kit (10 plate)

Neonatal Biotinidase kit is intended for the semi-quantitative determination of biotinidase activity in blood specimens dried on filter paper as an aid in screening newborns for biotinidase deficiency.
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Neonatal G6PD kit (10 plate)

Neonatal G6PD kits are intended for the semi-quantitative determination of glucose-6-phosphate dehydrogenase (G6PD) concentrations in blood specimens collected onto filter paper, as an aid in screening newborns for G6PD deficiency.
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Neonatal Biotinidase kit (50 plate)

Neonatal Biotinidase kit is intended for the semi-quantitative determination of biotinidase activity in blood specimens dried on filter paper as an aid in screening newborns for biotinidase deficiency.
PerkinElmer

Resolve Hemoglobin kit (360 tests)

The RESOLVE® Neonatal Hemoglobin test kit is designed to separate whole blood, cord blood or dried blood spot specimens for detection of normal and variant hemoglobins by isoelectric focusing.
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GSP Neonatal hTSH kit

Congenital hypothyroidism (CH) results from a failure of the thyroid glands to produce thyroid hormones in adequate amounts. The condition can easily be treated with daily doses of thyroid hormones but clinical diagnosis is difficult to establish and the disease may continue unrecognized for a long time causing irreversible brain damage.
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CHS MSMS Steroids Kit

CHS MSMS Steroids Kit
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AutoDELFIA Neonatal hTSH kit (12 plate)

This kit is intended for the quantitative determination of human thyroid stimulating hormone (hTSH) in blood specimens dried on filter paper as an aid in screening newborns for congenital (neonatal) hypothyroidism using the 1235 AutoDELFIA® automatic immunoassay system.
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AutoDELFIA Neonatal IRT kit (12 plate)

This kit is intended for the quantitative determination of human immunoreactive trypsin(ogen) (IRT) in blood specimens dried on filter paper as an aid in screening newborns for cystic fibrosis using the 1235 AutoDELFIA® automatic immunoassay system.
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MSMS Vitamin D Derivatization Box

The MSMS Vitamin D Derivatization Box is intended for in vitro diagnostic use with the MSMS Vitamin D Kit (3075-0010) to derivatize 25-hydroxyvitamin D2 and 25-hydroxyvitamin D3 for greater assay sensitivity.
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AutoDELFIA Neonatal Thyroxine (T4) kit (12 plate)

This kit is intended for the quantitative determination of human thyroxine (T4) in bloodspecimens dried on filter paper as an aid in screening newborns for congenital (neonatal) hypothyroidism using the 1235 AutoDELFIA® automatic immunoassay system.
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GSP Neonatal Total Galactose kit

The GSP® is a high throughput batch analyzer intended for quantitative or qualitative measurement of neonatal screening samples on 96-well microplates. The instrument is fully automated, performing every stage of an assay from retrieval of the sample plate from the stacker to measurement and reporting of results.
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NeoGram AAAC Tandem Mass Spectrometry kit

The Neogram MSMS kit is intended for the quantitative determination of up to 10 clinically significant amino acids and 13 clinically significant acylcarnitines, detecting up to 30 different metabolic diseases from a single dried blood spot sample using the MS/MS tandem mass spectrometer.
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NeoBase Non-derivatized Assay Solutions

The NeoBase MSMS kit is intended for the quantitative determination of up to 11 clinically significant amino acids and 31 clinically significant acylcarnitines, detecting more than 30 different metabolic diseases from a single dried blood spot sample using the MS/MS tandem mass spectrometer.
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NeoBase Succinylacetone Assay Solution

The NeoBase Succinylacetone Solution is intended for use with the NeoBase Non-derivatized MSMS Kit for the measurement and evaluation of succinylacetone from newborn heel prick blood samples dried on filter paper.
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GSP Neonatal IRT kit

The diagnosis of cystic fibrosis is often based on the symptoms, which may cause considerable delays in the disease intervention, and evidence indicates that early attention may be important in determining the clinical outcome.
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NeoGram Derivatized Assay Solutions

The NeoGram Derivatized Assay Solutions are intended for in vitro diagnostic use with the NeoGram Amino Acids and Acylcarnitines (AAAC) Tandem Mass Spectrometry Kit. The product includes NeoGram AAAC Flow Solvent, NeoGram AAAC Extraction Solution, NeoGram AAAC Reconstitution Solution and 3.0 N HCL in n-butanol.
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DELFIA® Neonatal hTSH kit (10 plate)

DELFIA Neonatal hTSH kits are intended for the quantitative determination of human thyroid stimulating hormone (hTSH) in blood specimens dried on filter paper as an aid in screening newborns for congenital hypothyroidism.
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MSMS Vitamin D kit

The MSMS Vitamin D Kit is an in vitro diagnostic high performance liquid chromatography tandem mass spectrometry (HPLC-MSMS) reagent kit, intended for the quantitative determination of 25-hydroxy-vitamin D2 and 25-hydroxy-vitamin D3 in human serum samples.
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NeoBase Non-derivatized Assay Solutions

The NeoBase Non-derivatized Assay Solutions are intended for in vitro diagnostic use with the NeoBase Non-derivatized MSMS Kit and the NeoBase Succinylacetone Solution. The product includes NeoBase Flow Solvent and NeoBase Extraction Solution.

"Newborn Screening Reagents" 1-43 of 43 Products and Services