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        EF10100 Electrophoretic KIT EXPRIME 72 ENG.
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1.  for  reagents dilution     PRECAUTIONS    Reagent may contain not reactive and conservative    components  It is opportune to avoid contacts with the  skin and do not swallow    Perform the test according to the general    Good  Laboratory Practice     GLP  guidelines    Pay attention to hazard symbols and R and S on the  labels  Consult the MSDS     PREPARATION AND STORAGE OF REAGENTS    The reagents not contaminated when stored at 4 30  C    in the dark are stable until the expiration date on the  label   The Staining is supplied ready for use     Buffer is provided concentrated 10 X    Dilute 1 10 with distilled water    The diluted buffer is stable 20 days at 15 25  C or 35  days at 2 8  C     Destaining is provided concentrated 20 X    Destaining can produce a precipitants  that are redissolved  by water bath at max  50 TC    Dilute 1 20 with distilled water    The diluted Destaining  not contaminated  is stable until  expiry date stated on the label     PROCEDURE    Loading Reagents   Place the bottle of Staining reagents on the instrument  compartment 72 EXPRIME ensuring the inclusion of  the loading pipe marked with the word  STAIN     The contents of the vial is sufficient for the correct color  of 25 cellulose acetate membranes    Fill the room electrophoresis instrument until to  indicated level  approx  150 ml   with Buffer diluted  previously prepared    Replace the buffer diluted every 25 tests  or in case of  any mold    Insert into the slots of the electropho
2. Meridiagkhlealtincare     TEST SUMMARY    The proteins in the samples are separated in the    appropriately buffered by electrophoretic migration    The result is achieved by depositing a serum sample on  a appropriate support of cellulose acetate with hard  plastic material and application of electric current to a  preset time    The protein fractions are positioned  individually  in  different areas of the strip according to their specific  electrical charge    Once correctly completed electrophoretic  migration    the strip should be treated with a reagent capable of  highlighting the protein fractions  and in this case you  use dye Red Ponceau S  At the end of the staining  process is necessary to remove excess dye to make  visible only the bands of protein fractions  this is  achieved by treating the strip with an appropriate  destaining  The strip is read by an optical scanner  system  The values are expressed as a percentage of  the different fractions  with the chart of the separation     SAMPLES    Serum not hemolized collected according to NCCLS    H11 A3 document   Stability 2 weeks at 2 8  C or 4 days at 15 25  C     REAGENTS   Buffer  Tris Hippurate buffer    Staining R P   Ponceau S 0 2   p v    Destaining  Citric Acid 1 M I  preservatives    and stabilizers  Electrophoretic stripes  cellulose acetate 76 x 60 mm     MATERIAL REQUIRED BUT NOT SUPPLIED    EXPRIME 72 instrument  Normal laboratory equipment    Distilled water  5 liters tank or fit plastic containers
3. TED VALUES  Albumin 3 6     4 9 g dl 55     64    Ot 0 2     0 4 g dl 2 2     4 5    Op 0 4     0 8 g dl 7     9    B 0 6     1 0 g dl 9     13    y 0 9     1 4 g dl 14   18   Every laboratory should establish own reference  intervals in accordance with own population   NOTES  e Use only throwaway materials for to avoid    contaminations    e  f the results are incompatible with clinical  presentation  they have to be evaluated within a total  clinical study    e Only for IVD use     CALIBRATION   QUALITY CONTROL    It is suggested to perform an internal quality control    with Control Serum of serum proteins     TEST PERFORMANCE    All the performance of this reagent were established on    the instrument EXPIME 72 using reagents     Methods comparison   46 samples of normal and pathological sera were  analyzed by electrophoretic LTA KIT EXPIME on 72  and the results were compared with those obtained with  a similar system commercially available    The LTA has confirmed KIT electrophoretic paths  equivalent to those of the reference system with a  100  agreement     Interferences  In Hemolyzed serum  free hemoglobin bound by  Haptoglobin interferes with the assay of Fraction Alpha  2  Are described in the literature various drugs and  other substances that may interfere with the  determination     Precision  Sample 1    B04   0422   416      Sample 2  o B   1079   o7   387    Ooo y o   2442   on7   29          WASTE DISPOSAL    Product is intended for professional laboratorie
4. cniche di  Chimica clinica p 672     MANUFACTURER    laboratorio     Meridian Healthcare srl    Tel   39 095 725 68 69 Fax    39 095 725 44 54    info meridianhealthcare  it  www meridianhealthcare  it    SYMB       OLS  Only for IVD use  Lot of manufacturing     lt        Code number   Storage temperature interval  Expiration date   Warning  read enclosed documents  Read the directions    e aa E    Biological risk  Mod  01 06  ver  1 3     24 01 2011     
5. resis chamber  the  Felts included in the kit  previously immersed in buffer  for 1 minute     ELECTROPHORETIC KIT  EXPRIME 72     Qualitative and quantitative determination of serum proteins  5 fractions  on EXPRIME 72 instrument    Insert the intake hose necessary to Destaining into the  tank containing the reagent previously diluted  Make  sure  when using the level of the tank never falls below  500 ml  Also make a 5 litres tank containing distilled  water  CLEAN  required for cleaning tool and 1 empty  tank necessary to drain  WASTE     Assemble the electrophoretic strip on the appropriate  frame  avoid handling the surface     WARNING  It is recommended to verify the correct  and complete tightening of carrier strips    Put the frame in the strips rack framed of the  instrument  starting from position 1    Place the filter paper into the slots  For instruments  equipped with automatic loading and unloading of  reagents fill the pan with the respective reagents  diluted    For details  see the user manual of the instrument     Loading Samples   Pipet 25 30 ul of fresh serum not hemolyzed each well  of the base sample holder  ensuring a homogeneous  distribution and without bubbles     Operations   Parameters    Constant current  Optics Compensation    IMBIBITION  DRYING 1  MIGRATION  STAINING  DESTAINING 1  DESTAINING 2  DRYING 2  DEPOSITION TIME    O    120 second   o0 second    720 seconds  1    20  150    second  a20 second  300 second  s second  20 second       EXPEC
6. s  Waste    products must be handled as per relevant security  cards and local regulations     PACKAGING   CODE EF10100  400 TESTS    Buffer 1x100mi  liquid   Destaining 2x250 ml  liquid   Staining 2x100ml  liquid   Electrophoretic stripes 2 x 25 pc    Imbibition set 4 pc    Paper set 10 pc    CODE EF10110  200 TESTS    Buffer 1 x 50 ml  liquid   Destaining 1x 250ml  liquid   Staining 1x100mi  liquid   Electrophoretic stripes 1 x 25 pc    Imbibition set 2 pc    Paper set 5 pc   REFERENCES    Young DS  Effects of drugs on Clinical Lab  Test  4 ed     AACC Press  1995    Young DS  Effects of disease on Clinical Lab  Test  4 ed   AACC Press  1999    M  Paget e Coustenoble  Microelectrophor  se des prot  ins  du s  rum sur acetate de Cellulose G  latineux Ann  Biol   Clin   23 10 12  1209 1219  1965     Kenz Stato and Haruko Kasai  Japan  Electrophoresis of  serum Proteins on gelatinized Cellulose Acetate Medicine  and Biology 70  5  195 298 May  10  1965      Medicine and  Biology 71  3  144 151 Spt  10  1965     B  Colfs     J  Verheyden  Rapid Method for Determination of  Serum Haptoglobin Clin  Chim  Acta 12     470 472  1965    G  Rapi     V  Frangini     C  Maggi     D  Pratesi  Elettroforesi  e Microelettroforesi R adiale su gel di acetato di Cellulosa    Proteine e Emoglobine   Riv  Clin  Pediatra     Vol  78     n   6  785 800  1966     J  Kohn  abstracts of VI Inter  Congr  Clin  Chemistry see  page 203 204 S  Karger A G   Basel  1966    F  Pasquinelli  Diagnostica e Te
    
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