El-Hiv4g Human Leaflet
El-Hiv4g Human Leaflet
El-Hiv4g Human Leaflet
C
Cat. No.
Component Quantity / Volume
51215 512155
[MIC] Microtiter strips 1x 5x 12 x 8-well strips, sealed in aluminium- foil bag,
labelled
[NC] anti-HIV 1/2, p24 1 x 2.5 ml 2 x 2.5 ml filled into round glass vial, closed with green
Negative Control screw cap, labelled
[PC-1] anti-HIV 1/2 Positive 1 x 2.0 ml 2 x 2.0 ml filled into round glass vial, closed with red screw
Control cap, labelled
[PC-2] p24 Positive Control 1 x 2.0 ml 2 x 2.0 ml filled into round glass vial, closed with white
screw cap, labelled
[CON-1] anti-HIV 1/2, p24 1 x 1.2 ml 1 x 3.6 ml filled into round brown glass vial, closed with
Conjugate yellow screw cap, labelled
[CON-2] HRP Conjugate 1 x 2.0 ml 2 x 2.0 ml filled into round brown glass vial, closed with blue
screw cap, labelled
[DIL-C1] Conjugate-1 Diluent 1 x 12 ml 3 x 12 ml filled into round transparent plastic vial, closed
with transparent screw cap, labelled
[DIL-C2] Conjugate-2 Diluent 1 x 20 ml 2 x 20 ml filled into round transparent plastic vial, closed
with transparent screw cap, labelled
[WS] Wash solution 1 x 50 ml 2 x 120 ml concentrate, filled into round transparent plastic
vial, closed with transparent screw cap, labelled
[SA] Substrate Reagent A 1 x 2.5 ml 3 x 2.5 ml concentrate, filled into round brown plastic vial,
closed with brown screw cap, labelled
[SB] Substrate Reagent B 1 x 25 ml 3 x 25 ml filled into round brown plastic vial, closed with
brown screw cap, labelled
[STOP] Stop Solution 1 x 25 ml 2 x 50 ml filled into round transparent plastic vial, closed
with transparent screw cap, labelled
Adhesive strips 2 10
1.5 Storage
All kit components have to be stored at 2...8°C. Freezing must be avoided.
1.6 Stability
HIV Ag/Ab ELISA is stable up to 24 months from the date of production when sealed and stored properly.
Performance Test
Specifications Results
This product met the quality control release criteria and has been released by the responsible
Quality Control Department of HUMAN GmbH.
Following release of the product, this certificate of analysis is electronically regenerated and
valid without signature.
Performance Test
Specifications Results
This product met the quality control release criteria and has been released by the responsible
Quality Control Department of HUMAN GmbH.
Following release of the product, this certificate of analysis is electronically regenerated and
valid without signature.