| Product Name: | Fetal Bovine SERUM (Dialyzed) |
| Product No.: | FB4501 |
| Cuntry of origin: | AUSTRALIA |
| TEST | METHOD | SPEASFICATION | RESULTS |
| Mycoplasma | Broth Culture 28 or 35 Day Incubation | Not Detected | Not Detected |
| Viruses: | 9CFR 113.53c | ||
| Bovine Respiratory Syncytial | Fluorescent Antibody | Not Detected | Not Detected |
| Bovine Viral Diarrhea Virus | Not Detected | Not Detected | |
| Bovine Parvovirus | Not Detected | Not Detected | |
| Bluetongue Virus | Not Detected | Not Detected | |
| Bovine Adenovirus | Not Detected | Not Detected | |
| Rabies Virus | Not Detected | Not Detected | |
| Reovirus | Not Detected | Not Detected | |
| Infectious Bovine Rhinotracheitis | Cytopathic Agents | Not Detected | Not Detected |
| Haemoglobin | UV/VIS Spectrophotometer | ≤0.2 mg/ml | 0.11 mg/ml |
| Endotoxin | LAL | ≤5 IU/ml | 0.07 IU/ml |
| Antibodies: | |||
| BVD | VNT | ||
| IBR | VNT | ||
| PI3 | Elisa | ||
| BT | Elisa (Australia) | ||
| pH | pH Meter | 7.35 | |
| Osmolality: | Osmometer | 306mOsmol/kg | |
| Total Protein | COBAS Fara Analyser | 3.5mg/ml | |
| Albumin | Electrophoresis | 2.1g/l | |
| Alkaline | Electrophoresis | 237U/l | |
| Phosphatase | |||
| ALT (SGPT) | Electrophoresis | 3U/I | |
| AST (SGOT) | Electrophoresis | 39U/I | |
| Bilirubin, Total | 0.1mg/dL | ||
| BUN | 0 mg/dL | ||
| Calclum | 0.85 mM | ||
| Chloride | 28.6 mM | ||
| Cholesterol | 38 mg/dL | ||
| Cortisol | 16.6 nM | ||
| Creatirnine | 0.4 mg/dL | ||
| Estrogen | 88.29 pM | ||
| Glucose | 0.1 mM | ||
| Hemoglobin | 11.8 mg/dL | ||
| Insulin | 19.79 pM | ||
| Phosphorus | 0 mM | ||
| Potassium | 0.7 mM | ||
| Progesterone | ＜0.16 nM | ||
| Sodium | 156 mM | ||
| M | 0.00 nM | ||
| T3 | 1.2 nM | ||
| T4 | 132.6 nM | ||
| Triglycerides | 6 mg/dL | ||
| Tetracycline | ＜0.5 μg/mL | ||
| Uric Acid | 0.3 mg/dL |
Results shown were obtained by carefully performed methods believed to be reliable. However, since some results may vary by methodology, it is suggested that tests for which results are particularly critical be repeated by the end user. Our fetal bovine serum meets all USDA requirements and has passed ante- and post-mortem inspection by a licensed veterinarian. It is collected in countries recognized as being free of foot-and-mouth disease and rinderpest. The origin of all fetal bovine serum is traceable by lot number, date and country of collection. Precipitates may develop in this product upon freezing and/or thawing; this occurrence does not impact culture performance.