SERUM
PROTEINS (100 semimicro or 200 micro tests)
CODE 08C30-R
The kit is
intended fot the diagnostic clinical electrophoresis of serum
proteins for detecting disproteinemias and for quantitating
Albumin, Alpha-1, Alpha-2, Transferrin, C3 and Gammaglobulins.
Assessment:
4 semimicro or 8 micro tests per each Cellogel 5.7x14 cm strip.
12 semimicro tests or 24 micro tests per each Cellogel chamber.
Kit content:
Cellogel, Tris-Hippurate buffer, Ponceau S staining, Destaining
solution, Clearing solution, blotting paper and Mylar film |
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HIGH RESOLUTION
SERUM PROTEINS (150 semimicro or 200 micro tests)
CODE 08C31
Several prestigious authors (Drs. Kohn, Laurell,
Aguzzi, Keren et. al.) have not accepted the 20 mm micro electrophoresis
of proteins since this technique is not sufficient for diagnosis
of gammapathies. HR methods such as Microlong electrophoresis
on Cellogel show up to 13 fractions, and have been proposed
for diagnosis of incipient gammapathies. In accordance with
the Italian Commission for Proteins of SIBioC and some of
the most authoritative European experts.
Assessment:
6 semimicro or 8 micro tests per each Cellogel 5.7x14 cm strip.
48 high resolution tests with 6 Cellogel strips placed on
2 Cellogel chamber.
Kit content:
Cellogel, TGS buffer, Coomassie staining, Citric Acid, Clearing
solution blotting paper and Mylar film.
Materials not included: Destaining solution (475ml
Methanol + 475ml H2O
+ 50ml Glacial Acetic Acid).
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| IFE
SERUM + CONCENTRATED URINE (5+5 tests for 5 patients)
CODE 08C09
Simultaneous
immunofixation of serum and urine of 1 patient is recommended
as unique method for an absolutely certain diagnosis able
to observe gammapathies of uncertain significance (MGUS) or
the malignancy of the gammapathy, with the presence of a K
free or Lambda free monoclonal, or secondary malignancy for
evident kidney disease with the presence of an IgG, IgA or
IgM monoclonal component in the IFE of serum and urine with
relative positivity of alligned K (bound) or Lambda (bound).
This method, proposed in 1984 and appreciated from many SIBioC
members, doesn’t use anti K free and anti Lambda free
to reveal Bence-Jones protein and respects the guide lines
for IFE of the Bence-Jones proposed for urine alone with trivalent
anti-serum (anti IgG, anti IgA, anti IgM), anti K Bound &
Free and anti Lambda Bound & Free published in Biochimica
Clinica, 2001, vol.25, No. 1, pages 23-31.
Assessment:
2 test HRE for each patient in semimicro technique on 6 Cellogel
2.5x14 cm strip placed on 3 bridges in one Cellogel chamber.
Kit content:
Cellogel, TGS buffer, Coomassie staining, Saline solution,
Volumetric distributors and Antisera, Clearing solution, blotting
paper and Mylar film.
Materials not included:
Destaining solution (475ml Methanol + 475ml H2O
+ 50ml Glacial Acetic Acid). |
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| IMMUNOFIXATION
(24 semimicro or 32 micro tests)
CODE 08C09-2
The kit is
intended for the separation and identification of monoclonal
gammapathies. When a monoclonal band is revealed by electrophoresis
or when an immunoproliferative disorder is suspected, immunofixation
of monoclonal components is basic, either to establish true
monoclonality of a band, or to establish the nature of the
monoclonal component and fix it. In fact different types have
different diagnostic and prognostic value.
Assessment:
6 semimicro tests or 8 micro tests on 6 Cellogel 5.7x14 cm
strips placed on 6 bridges in two Cellogel chamber.
Kit content:
Cellogel, Tris- Hippurate buffer, Amidoblack staining, Saline
solution, Volumetric distributors and Antisera, Clearing solution,
blotting paper and Mylar film.
Materials not included:
Destaining solution (475ml Methanol + 475ml H2O
+ 50ml Glacial Acetic Acid). |
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HEMOGLOBINS
(100 semimicro tests)
CODE 08C35
Electrophoresis
of Hemoglobins is a simple laboratory technique for the rapid
and accurate detection of abnormal conditions, called hemoglobinopathies.
It can reveal the possible existence of hemoglobinopathies
in two ways, qualitatively, by indicating the presence or
absence of variant hemoglobins, and quantitatively, by making
possible the measurement of hemoglobins by densitometry.
The electrophoretic separation of hemoglobins is based on
the electrical characteristic of the globin molecule which
can be negatively or positively charged depending on the amino
acid sequence or composition of the polypeptide chains. Differences
in the electrostatic charge will produce differences in electrophoretic
mobilities and, hence, separation of the various hemoglobins.
Assessment:
4 semimicro per each Cellogel 5.7x14 cm strip.
12 semimicro tests per each Cellogel chamber.
Kit content:
Cellogel, Tris-Glycine buffer, Ponceau S staining, Destaining
solution, Clearing solution, blotting paper, Mylar film and
1 mini box. |
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GLYCOSYLATED
HEMOGLOBINS HbA1c (100 semimicro tests)
CODE 08C64
According
to a publication of J. Ambler et al., the non-glycosilated
part of Hemoglobin in citrate buffer pH 6.4 containing dextrane
sulphate acquires a mobility such as to allow a perfect separation
of the glycosilated part. This occurs as the sulphate groups
of dextrane combine with non-glycosilated hemoglobin.
Assessment:
4 semimicro per each Cellogel 5.7x14 cm strip.
12 semimicro tests per each Cellogel chamber.
Kit content:
Cellogel, Affinity buffer pH 6.4, Hemolysing solution, Ponceau
S staining, Destaining solution, Clearing solution, blotting
paper, Mylar film and 1 mini box. |
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LIPOPROTEINS
(100 semimicro tests)
CODE 08C42
The Kit is intended for clinical electrophoresis
of serum Lipoproteins and evaluation of HDL (Alpha lipo),
VLDL (pre ß lipo), LDL (ß lipo) and Chylomicrons
fractions.
Hyperlipoproteinemias may be categorized into 5 types according
to Fredrickson et Al. by simple observation of electrophoretic
pattern, serum appearance and determination of values of Cholesterol
and Tryglyceride.
Cellogel is widely used in the world for Lipoproteins testing.
More than 20 scientific works have been published on international
magazines. Main advantage of Cellogel versus dry Cellulose
Acetate or Agarose is the right porosity (Chylomicrons can
not penetrate or permeate Cellogel membrane), the suitable
thickness of 250-300 microns and combination of both hydrophobic
and hydrophilic properties of gelatinized cellulose acetate.
Assessment:
4 semimicro per each Cellogel 5.7x14 cm strip.
12 semimicro tests per each Cellogel chamber.
Kit content:
Cellogel, Tris Hippurate buffer, Sudan Black staining, Clearing
solution, blotting paper, Mylar film and 1 mini box.
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