BRO MSMS NeoLSD Kit 1599-9813-03 LR
BRO MSMS NeoLSD Kit 1599-9813-03 LR
BRO MSMS NeoLSD Kit 1599-9813-03 LR
EFFICIENT
LSD
SCREENING
SCREENING
screening since 2002, currently offers the NeoBase™ Non-derivatized MSMS Kit, the
commonly used reagent in mass spectrometry based testing for amino acid, organic
acid, and fatty acid oxidation disorders, used to screen millions of babies annually.
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KIT INCLUDES ALL EASY ASSAY WORKFLOW
NECESSARY ITEMS
FOR EFFECTIVE OR OR
LSD NEWBORN
SCREENING Assay
Punch
1
Add Cocktail
2
Shake & Incubate
3
Quench & Mix
3.2 mm DBS Add 30 µL 37°C, 400 rpm Remove seal, add 100
to 96-well plate Cocktail, seal 18 ± 2 hours µL 50:50 MeOH:EA,
mix w/pipette.
KIT INCLUDES:
Package P1 Package P2 Package P3
NeoLSD Substrates and Internal Neo MSMS Flow Solvent Microplate, Deep
Standards (5 vials, dried) (1 bottle, 800 mL) Well (10 plates)
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Barcode labels for the Adhesive aluminum foil
plate (30 pcs) Transfer Liquid & Extract
microplate covers (20 sheets)
Separate Layers TransferTransfer
Liquid &Top Layer
Extract Separate Layers TransferTransfer
Liquid &Top Layer
Extract Separate Layers
To deep 96-well plate (DWP). Add 400 µL DWP centrifuge, 2 min To deep 96-wellTransfer
plate (DWP).
100 µL Add
of 400 µL DWP centrifuge, 2 min To deep 96-wellTransfer
plate (DWP).
100 µLAdd
of 400 µL DWP centrifuge, 2 min
EA & 200 µL H2O Mix with pipette. EA & 200 µL
topH2O
layerMix with pipette.
to sampling EA & 200 µL
topH2O
layerMix with pipette.
to sampling
Lot-specific quality control Adhesive microplate plate plate
certificate (1pc) covers (10 sheets)
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EFFICIENT NEWBORN SCREENING
RUN UP TO The following data illustrates representative performance with the Waters® Xevo® TQD instrument.
500
Enzyme activity (µmol/L/h)
Enzyme n Lower percentiles
Range Mean Median
0.5th 1.0th
ABG 1981 2.48-52.0 11.19 10.31 3.52 3.89
ASM 1981 1.30-35.1 7.12 6.63 2.66 2.95
GALC 1981 0.30-42.2 4.68 3.91 0.79 0.97
KEY FEATURES:
Import data from instrument software Sample and assay audit tracking
- Concentrations, IS intensties and TIC raw data
Automatic export to R4S for analysis
Automatically perform LSD specific calculations
Export results to LIMS
Visualize results
- Plate map with colored wells
- Flagging of wells violating cutoffs or other QC criteria
- View TIC & spectra
- View results by disorder
- Split grid view for easy review of results
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COMPLETE MASS SPECTROMETRY
SOLUTIONS FOR NEWBORN SCREENING.
A COMMUNITY OF SUPPORT
From dried blood spot cards, punchers, instruments, reagents to informatics, PerkinElmer's mass spectrometry
solutions empower newborn screening laboratories across the globe to meet their demands.
By joining the PerkinElmer newborn screening community, you become part of a movement that includes the
majority of the newborn screening laboratories and leaders worldwide. In addition to all necessary equipment,
reagents and informatics, we also provide on-site installation and training, ongoing support, phone consults and
various training courses. We are here to help you improve your newborn screening program.
LSDs comprise a heterogeneous group of nearly 50 disorders observation can be difficult. Enzyme replacement therapy or
that are caused by genetic defects resulting in the dysfunc- hematopoietic stem cell transplantation are available to treat
tion, deficiency or absence of a lysosomal enzyme. Although some LSDs, however, if an available therapy is delayed, irre-
each disorder is rare, LSDs as a group have a frequency of versible tissue damage may result.
1 in 7,000-8,000 live births. Affected individuals are unable
to metabolize the disease specific substrate of the deficient Infantile onset forms of some LSDs (Pompe and Krabbe disease)
lysosomal enzyme, which leads to progressive accumulation may be fatal within the first year of life when left untreated.
of the substrate in the lysosomes of tissues. Mutations that Early diagnosis and treatment is essential to the wellbeing of
result in an LSD are highly heterogeneous. Affected individ- individuals with these diseases.
uals exhibit a broad variety of disease severities with wide-
spread symptoms and ages of onset. Because symptoms are
absent at birth, early diagnosis of these diseases by clinical
Products may not be licensed in accordance with the laws in all countries, such as Canada.
Please check with your local representative for availability.
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