BeNa Culture Collection
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| Culture medium | Special peptone: 23.0, soluble starch: 1.0, sodium chloride: 5.0, agar: 10.0,pH:7.3±0.2(25 ℃) |
| Subculture procedure | Remove from the refrigerator, melt completely, vortex and mix well, ready to use. Note: The quality control is inactivated particles, which need to be used after nucleic acid extraction. The extraction or purification reagents should be prepared by themselves, and repeated freezing and thawing should be avoided before extraction. The minimum sampling volume is 200 μl. |
| Growth conditions | 37 ℃;18-24h; aerobic |
| Storage conditions | -80 ℃ |
| Safety level | 1 |
| morphology | The colony diameter is 0.5-1mm, round, opaque, gray-white on the front, raised in the middle, smooth surface, dry texture, G (blue-purple), cocci |
| Separation substrate | Human urine, 13-yr-old boy |
| application | Related research on nucleic acid detection reagents for pathogens |
| Sharing mode | Public welfare sharing |
Rothia mucilaginosa nucleic acid reference (Heat inactivated) (Strongly positive)(Rothia mucilaginosa nucleic acid reference (Heat inactivated) (Strongly positive))
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Rothia mucilaginosa nucleic acid reference (Heat inactivated) (Strongly positive)(Rothia mucilaginosa nucleic acid reference (Heat inactivated) (Strongly positive))
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Rothia mucilaginosa nucleic acid reference (Heat inactivated) (Strongly positive)(Rothia mucilaginosa nucleic acid reference (Heat inactivated) (Strongly positive))
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