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REAGENT/SUPPLY SPECIFIC TEST DESCRIPTION

Randox reagent Albumin The Randox reagent


comes in a liquid format
which is more convenient
https://www.randox.com/ as the reagent does not
albumin/ need to be reconstituted
which aids in reducing the
risk of errors occurring.
The normal values of
Albumin in serum is 38 –
44 g/l in adults and 38 –
42 g/l in neonates. The
Randox reagent is highly
sensitive and can
comfortably detect as low
as 2.87 g/l of Albumin
within a sample.Albumin is
a special protein made in
the liver and provides the
body with the proteins it
requires to grow and
repair tissue. The body
requires a proper balance
of albumin to prevent fluid
from seeping out of blood
vessels.The Randox
Albumin test allows for
timely and accurate
assessments of kidney
disease; resulting in the
correct adjustment of
treatment and accurate
monitoring of the
complications of diabetes.

Burchard reagent (the Cholesterol the LiebermannBurchard


LiebermannBurchard and and Zak reactions have
Zak reactions) found the widest
application in clinical
analysis. Cholesterol was
allowed to react with
sulphuric acid and acetic
anhydride in chloroform
solvent in the original
studies, but the
Liebermann-Burchard
reaction is now carried out
in an acetic acid-sulphuric
acid-acetic anhydride
medium. The Zak reaction
carried out in an acetic
acid-sulphuric acid
medium. In this reaction,
however, ferric ions must
be present to obtain the
required coloured species
as explained below.

Creatinine reagents: 1. Creatinine is reacted


with 3,5-dinitrobenzoate
1. Alkaline
under alkaline reaction
3,5-dinitrobenzoate
conditions to produce a
2. 3,5-dinitrobenzoyl fluorophore. Alternatively,
chloride 3,5-dinitrobenzoyl
chloride or
methyl-3,5-dinitrobenzoat
e may be employed as
reagents. Fluorophore
development was
evaluated for Group IA
bases under aqueous and
mixed solvent conditions.
To develop a new
quantitative fluorometric
assay for creatinine with
enhanced specificity and
inherent fluorescence
sensitivity.
2.

Creatinine enzyme buffer Creatinine enzymatic 1. The VITROS CREA Slide


reagents: is a multilayered,
analytical element coated
1. Vitros Crea Slides
on a polyester support. A
https://www.accessdata.f drop of patient sample is
da.gov/cdrh_docs/pdf6/K deposited on the slide and
is evenly distributed by
063591.pdf the spreading layer to the
underlying layers.
Creatinine diffuses to the
2. Olympus Roche reagent layer, where it is
hydrolyzed to creatine in
3. Randox
the rate-determining step.
The creatine is converted
to sarcosine and urea by
creatine
amidinohydrolase. The
sarcosine, in the presence
of sarcosine oxidase, is
oxidized to glycine,
formaldehyde, and
hydrogen peroxide. The
final reaction involves the
peroxidase-catalyzed
oxidation of a leuco dye to
produce a colored
product. Following
addition of the sample,
the slide is incubated.
During the initial reaction
phase, endogenous
creatine in the sample is
oxidized. The resulting
change in reflection
density is measured at 2
time points. Once a
calibration has been
performed for each slide
lot, creatinine
concentration in unknown
samples can be
determined using the
softwareresident
two-point rate math
model and the change in
reflectance calculated for
each unknown test slide.
2.

Direct Bilirubin Reagent D Bilirubin A reaction in which


bilirubin is coupled with
http://www.pointescientif diazotized sulfanilic acid
ic.com/uploads/inserts/B7 (ρdiazobenzenesulfonic
538-01-847.pdf acid) to produce an azo
dye was first described by
Ehrlich in 1884.1 The
color of this derivative is
pink in an acid medium
and blue in an alkaline
one. The measurement
of the blue form has been
more popular because of
greater sensitivity, etc.
Two types of serum
bilirubin can be
distinguished and
quantitated by the diazo
reaction. The direct
form, consists of
conjugated, water-soluble
derivatives and reacts in
the absence of an
accelerating or solubilizing
agent. The indirect form,
consists of free,
unconjugated bilirubin
bound to serum albumin.
This form reacts quickly in
the presence of an
accelerating agent. The
sum of these two forms is
termed total bilirubin. The
differentiation between
direct and indirect is
important in diagnosing
causes of
hyperbilirubinemia.

Urinalysis Reagent Strip Glucose Urinalysis test strips are


easy to use, cost-effective
https://www.surescreen.c medical tool that allow for
om/products/health/urina the specific diagnosis and
lysis/11-parameter-urinaly effective treatment of
sis-reagent-test-strips-50-s
trips/ various disease states. The
test strips are designed to
detect small pathological
changes in urine, and
provide the result via a
colour-change test field.
A strip is dipped in to a
urine sample, then using
the provided colour chart,
the results are matched to
ascertain concertation
levels of substances within
the urine. Test result may
provide information
regarding the status of
carbohydrate metabolism,
kidney and liver function,
acid-base balance, and
urinary tract infection.
Any irregular results
should be confirmed with
additional laboratory
testing of the urine
sample.

UV-Vis Glucose UV UV / Vis


Spectrophotometer spectrophotometer uses
visible light and ultraviolet
http://www.acttr.com/en/
to analyze the chemical
en-faq/en-faq-uv-vis/128-
structure of substance. A
en-faq-what-is-uv-vis-spec
spectrophotometer is a
trophotometer.html
special type of
spectrometer, which is
used to measure the
intensity of light, and the
intensity is proportional to
the wavelength. When
ultraviolet project to
various organic
compounds, these
compounds will absorb it.
So, you can use UV / Vis
spectrophotometer to
measure the absorption of
a compound by the result,
and have its molecular
structure, as well as the
related information. UV /
Vis spectrophotometer
has two types,
single-beam and
dual-beam. The
single-beam UV-Vis
spectrophotometer has
only one cuvette,
therefore, the Treatment
Group and the Control
Group samples can one be
measured one after the
other. With the
double-beam UV-Vis
spectrophotometer, you
can measure the both
groups simultaneously. So
that the double beam
UV-Vis spectrophotometer
is more accurate, because
you don’t need to
recalibrate the
instrument, before you
measure the second
sample.

HDL precipitating reagent HDL Direct

http://www.diatron.com/clinical-chemistry-reagents

SUBSTRATES
o Albumin
o Cholesterol
o Creatinine
o Creatinine Enz
o D Bilirubin
o Glucose
o Glucose-UV
o HDL Direct
o LDL Direct
o T Bilirubin
o T Protein
o Triglycerides
o UIBC
o Urea
o Uric Acid
o Urinary Protein (CSF)

ENZYMES
o ACE
o ADA
o ALP
o ALT/SPGT
o Amylase
o AST/SGOT
o Cholinesterase
o CK-MB
o CPK
o G6PDH
o g-GT
o LDH L>P
o LDH P>L
o Lipase

ELECTROLYTES
o Calcium
o CO₂
o In Phosphorous
o Iron
o Magnesium
o Potassium
o Sodium
o Lithium
o Chloride

SPECIFIC PROTEINS
o APO A1
o APO B
o ASO
o C3
o C4
o CRP Latex
o CRP
o Cystatin C
o D-Dimer
o Ferritin
o HbA1c
o Hb A1c denaturant
o IgA
o IgG
o IgM
o Lp(a)
o Microalbumin
o RF Latex
o Transferrin
o sTfR

CONTROLS AND CALIBRATORS


o ACE Cal
o ACE Control
o ADA Cal
o ADA Control
o Apo-A1/APO-B Cal
o APO-A1/APO-B Control level 1
o APO-A1/APO-B Control level 2
o Medi-Cal Chemistry Cal
o CC Control level 1
o CC Control level 2
o ASO Calibrator
o CRP Calibrator
o Ferritin Calibrator
o RF Calibrator
o Protein
o Immunology control 1
o Immunology control 2
o Immunology control 3
o LP(a) Calibrator
o LP (a) control low
o LP (a) control high
o D-Dimer Calibrator
o D-Dimer Control
o CRP Latex Calibrator
o Ethanol Control
o Ethanol Calibrator
o HbA1c Calibrator
o HbA1c Control
o sTFR Calibrator
o sTFR Control
o CK-MB Control
o CK-MB Calibrator
o Cystatin Control
o Cystatin Calibrator
o Ammonia Calibrator
o Ammonia Control
o G6PDH Control

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