MicroQuant™ Penicillium rubens, high CFU (Pack of 5)

MicroQuant™ strains are best-in-class controls developed to support USP General Chapters. These precisely quantitated controls are provided in a single-use format that rehydrates immediately and is easy to use and convenient to store. MicroQuant™ strains are direct from ATCC—passage zero.

MicroQuant™ Penicillium rubens, high CFU (ATCC 11709-HQ-PACK™) is provided as spores.

High-yielding, sporulating, penicillin strain

The strain was re-identified as Penicillium rubens, a close sister of Penicillium chrysogenum, based on the multigene sequence analysis.

1. Remove the desired number of cryopreserved reference culture vials (gray crimp) and rehydration buffer vials (green crimp) from 2-8°C storage and place into a biosafety cabinet. One vial of rehydration buffer should be used for each vial of reference culture.
2. Uncap each vial. Add 0.5 mL of rehydration buffer to the reference culture vial. Recap the vial and allow the pellets to dissolve for 30 seconds. Note: To ensure that an optimal titer range is maintained throughout the 8-hour post rehydration usability window, a 0.5 mL fill volume is used.
3. Vortex on the high setting for 30 seconds to ensure the suspension is well mixed. The suspension is now useable and contains 10⁷ to 10⁸ CFU per mL. The suspension can be used immediately or stored at 2-8°C for up to 8 hours. Note: Before plating, gently pipette the suspension up and down five times to ensure thorough mixing. If the suspension has been left standing for more than five minutes, or if it was stored at 2–8°C after rehydration, vortex the suspension again to ensure uniformity prior to use.
4. If this product is used in alignment with USP <51> guidelines, add 100 µL of the above prepared suspension to 900 µL of the test sample. 
5. Add 9.0 mL of the USP recommended diluent (not provided) to the 1.0 mL of sample prepared in step 4. Follow the procedure detailed in USP Chapter <51> for the challenge test.

For quantitation

1. Follow steps 1-3 listed above.
2. Add 100 µL of the prepared suspension to 900 µL dilution buffer (1x PBS + 0.01% Tween 80).
3. Repeat the dilution 4 times to achieve a dilution factor of 1.0 x 10⁵. 
4. From the final dilution, pipette 100 µL directly on to a non-selective media plate. Use a sterile plate spreader for optimal results. Note: ATCC quantitation results were obtained using 100 mm diameter Tryptic Soy Agar plates with 1.5% Tryptone, 0.5% Soytone, 0.5% Sodium Chloride, and 1.5% Agar (plates were procured from Teknova). Note: Sabouraud Dextrose Agar (SDA) may be used as well if appropriate for the organism.
5. Incubate plates in an incubator at the appropriate temperature and time. If following a specific pharmacopeial chapter, use the incubation conditions specified. 
6. Following incubation, read the plate for CFU counts using a standard colony counting procedure.

For applications outside of compendial assays, please refer to the product page for ATCC 11709 for standard growth conditions.

The product is provided 'AS IS' and the viability of ATCC^® products is warranted for 30 days from the date of shipment, provided that the customer has stored and handled the product according to the information included on the product information sheet, website, and Certificate of Analysis. For living cultures, ATCC lists the media formulation and reagents that have been found to be effective for the product. While other unspecified media and reagents may also produce satisfactory results, a change in the ATCC and/or depositor-recommended protocols may affect the recovery, growth, and/or function of the product. If an alternative medium formulation or reagent is used, the ATCC warranty for viability is no longer valid.  Except as expressly set forth herein, no other warranties of any kind are provided, express or implied, including, but not limited to, any implied warranties of merchantability, fitness for a particular purpose, manufacture according to cGMP standards, typicality, safety, accuracy, and/or noninfringement.

This product is intended for laboratory research use only. It is not intended for any animal or human therapeutic use, any human or animal consumption, or any diagnostic use. Any proposed commercial use is prohibited without a license from ATCC.

While ATCC uses reasonable efforts to include accurate and up-to-date information on this product sheet, ATCC makes no warranties or representations as to its accuracy. Citations from scientific literature and patents are provided for informational purposes only. ATCC does not warrant that such information has been confirmed to be accurate or complete and the customer bears the sole responsibility of confirming the accuracy and completeness of any such information.

This product is sent on the condition that the customer is responsible for and assumes all risk and responsibility in connection with the receipt, handling, storage, disposal, and use of the ATCC product including without limitation taking all appropriate safety and handling precautions to minimize health or environmental risk. As a condition of receiving the material, the customer agrees that any activity undertaken with the ATCC product and any progeny or modifications will be conducted in compliance with all applicable laws, regulations, and guidelines. This product is provided 'AS IS' with no representations or warranties whatsoever except as expressly set forth herein and in no event shall ATCC, its parents, subsidiaries, directors, officers, agents, employees, assigns, successors, and affiliates be liable for indirect, special, incidental, or consequential damages of any kind in connection with or arising out of the customer's use of the product. While reasonable effort is made to ensure authenticity and reliability of materials on deposit, ATCC is not liable for damages arising from the misidentification or misrepresentation of such materials.

Please see the material transfer agreement (MTA) for further details regarding the use of this product. The MTA is available at www.atcc.org.