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Quality Control Specifications
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Sterility tests are performed on each lot of calf bovine serum using current USP and EP methods. Each lot is also checked for its ability to support the growth of cells. Specific testing for contaminants is listed below in the Specification Certificate.
Origin
This fetal bovine serum is manufactured from fetal bovine blood collected in USDA-inspected abattoirs located in the United States.
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Test*
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Specification
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Sterility Testing (Current USP and EP)
Bacteria and Fungi
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No growth
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Virus Testing (9 CFR 113.53)
Fluorescent antibody
Bluetongue
Bovine Adenovirus
Bovine Parvovirus
Bovine Respiratory Syncytial Virus
Bovine Diarrhea Virus
Rabies
Reovirus
Cytopathogenic Agents (e.g. IBR)
Hemadsorbing Agents (e.g., PI3)
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Not detected
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Mycoplasma Testing
Large volume, direct culture Hoechst DNA stain
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Pass
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| Hemoglobin (spectrophotometric) |
≤ 20 mg/dL |
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Endotoxin (Limulus Amebocyte Lysate - Gel Clot)
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≤ 10 EU/mL
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Mycoplasma
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Pass
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Growth Promotion
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Pass
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*Please consult the Certificate of Analysis for lot-specific test results.
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