Portable Lab 2.5L Anaerobic Jar Price / Anaerobic Jar Various Discs Size for laboratory Microbial Anaerobic
Anaerobic Jar AG Series
DESCRIPTION
AG series anaerobic jar can be used with 2.5L AnaeroGen/CampyGen/Microaerobic sachet. It also can be fitted with MARK or DWS A05050 anaerobic system.
FEATURES: 1. No catalyst required.
2. Polycarbonate base which is secured to the lid by four clips. These clips are designed to allow venting in the unlikely event of a positive pressure build-up occurring i.e. by allowing lid to lift and reseal to maintain correct condition.
3. Vacuum relief screw to overcome any vacuum which may occasionally occur.
4. It can choose two different connectors to fit with all kinds of anaerobic system or flow with
gas.
Temperature resistance: can withstand no more than 100C high temperature Sealing: good sealing performance, anaerobic holding time not less than 120 hours
Locking: unique four-button seal design, simple operation, convenient, can be individually replaced lock, low maintenance costs
Can lid: 3 standard fitting holes are configured. Can be fitted with a connector to connect various anaerobic culture systems,
Use as a vent hole.
Material: The tank body and cover are made of transparent high-strength polyester material, high finish, shock and shock resistance
Temperature resistance: can withstand temperature 50C
Material: stainless steel (SUS304), durable, good thermal conductivity Temperature resistance: Can be resistant to 121C high temperature sterilization
Number of locks: 3
Product size: 19.7*13.5*9.5cm
Volume : 10 discs (diameter 90mm) max,
Method 1: operation with gas generating(Gas pack-kits)
1. Please check ‘O’ ring is correctly seated. And the vacuum relief screw is in the closed position.
2. Place inoculated plates into the plate carrier. Disposable plastic dishes should be of the vented variety to aid gas transfer between interior and exterior of the dishes.
3. Insert the anaerobic indicator to the upper clip on the dish carrier.
4. Lower the carrier into the polycarbonate base.
5. Tear open an sachet at the tear-nick indicated, and remove the paper sachet from within.
6. Immediately place the paper sachet in the appropriate clip in the plate carrier within the jar.
7. Having inserted the sachet into the carrier immediately place the lid on the jar, making sure the ‘O’ring is in the place. Secure the clips with fingers.
8. Transport the jar to the incubator.
9. The anaerobic indicator will change from blue the pink giving a visual indicationof anaerobiosis.
10. Remove jar after the appropriate incubation time and open lid by carefully depressing the clips to release the jar lid from base. Excessive downward pressure on the clips should beavoided.
11. Occasionally a slight vacuum may occur after anaerobiosis producing a negative pressure, resulting in resistance to the removal of the lid (after release of clips). This is overcome by screwing and turning anticlockwise allowing inlet of air. It is important, however, to ensure the valve is resealed by turning clockwise prior to further use.
1. Insert the carrier in the jar.
2. Place an anaerobiosis indicator in the jar.
3. Close the lid.
4. Connect the vacuum pump with a thick-walled hose to the connector.
5. Connect a gas bottle containing the requested gas mixture to the another connector. The pressure reduction valve is to set to max. 0.1 bar over pressure at the outside.
6. Open the valve connector with the pump and extract the gas from the jar.
7. Close the valve connector with the pump and open the valve connected with gas bottle.
8. Fill the jar with requested gas mixture up to 0.1 bar.
9. Depending on the sensitivity of the microorganisms, the process of evacuation and filling with gas may be repeated once or twice.
10. After the last filling with gas, close both valves and remove the hoses.
11.Transport the jar to the incubator.
1. Insert the carrier in the jar.
2. Place an anaerobiosis indicator in the jar.
3. Close the lid.
4. Connect a gas bottle containing the requested gas mixture to the connector. The pressure reduction valve is to set to max. 0.1 bar over pressure at the outside.
5. Open both two valve connector.
6. Open the gas supply and flow the jar with the requested gasmixture.
7. Flow the jar with requested gas mixture up to 0.1 bar overpressure.
8. Depending on the sensitivity of the microorganisms, the jar may be flowed from 5 to 15minutes.
9. After the last flowing with gas, close both valves and remove the hoses.
10.Transport the jar to the incubator.
The jar should not be autoclaved. It is not suitable incubator exceeding 80 celsius.
The Anaerobic jar only be wiped with alcohol as longer residence times may expand the material and cause cracks.
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