Quantitative strain of Pseudomonas aeruginosa|353739 |BNCC

Essential Information Certificate Related Products

Quantitative strains of pseudomonas aeruginosa

Growth conditions	37 ℃, 18-24h, aerobic;
Storage conditions	-20 ℃
Safety level	1
morphology	Round, opaque, gray white on the front, raised in the middle, smooth on the surface, bright on the surface, moist texture, easy to pick up
Sharing mode	Public welfare sharing

Pseudomonas aeruginosa

No.: 353739 / CMCC 10104

Product format : quantitative bacteria tablets

Number of live bacteria : 1.0~1.5×10 3CFU/bottle

Product batch : 191203

Balid until : 2020.6.2

Date of inspection : 2019.12.4

Sampling ratio : ≥2%

Report number : RS19353739-1

Biosafety level : 2 , handle in safety cabinet

Item	description	test results
stain microscopy	gram-negative and positive, cell morphology observed under microscope	G + cocci
colony morphology	observation of single colony morphology	light pink, translucent, producing pyogenin
purity	non-selective medium culture, colony observation and microscopic examination	No bacteria
Reference value of live bacteria	non-selective medium plate, live bacteria count	1110CFU/bottle
phenotype and genotype analysis	phenotypic testing, gene sequencing	qualified
test conclusion	after quality inspection by BNCC quality control testing system, the product is qualified

Product list :1.0~1.5 & times;10 3CFU quantitative strain 1 bottle, 1mL dissolved solution 1 bottle, strain certificate 1 copy;

Validity period: unopened, below -20 ℃, 6 months;

Handling procedure:

1 Open the penicillin-bottle according to the arrow indication on the vial cap;
2 Transfer the strain tablets into the vial of solution, capped with rubber plug, and shake to dissolve
3 It will be1.0~1.5×10 3cfu/ml after full dissolved, and use appropriate amount according to the operation demand
4 The bacterial tablets shall be used up once and shall not be retained once the penicillin bottled is opened.

Notes:

1 This product is a quantitative strain. Improper storage conditions and handling procedure will affect the accuracy of the strain quantities. Therefore, please operate in strict accordance with the above mentioned instructions.
2 Waste generated from the handling process should be discarded after high-pressure sterilization

Download certificate