CERTIFICATE OF ANALYSIS Not For Official Use
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CertifiCate of analysis
Not For
Official
Use
COA-2
GENERAL/STERILITYTEST METHOD RESULTS SPECIFICATIONHemoglobin UV/Vis Spectrophotometer ≤ 15 mg/dLEndotoxin Kinetic Turbidmetric ≤4 EUmLVisual examination Visual Satisfactory
Specificity Species I.D. BovineSterility Millipore Steritest - Broth
CultureSterile
Mycoplasma Broth Culture 35 day Incuba-tion
Not Detected
VIRUSES (9CFR 113-53C) RESULTS SPEC.Bovine Respiratory Syncytial Virus N.D.
Bovine Viral Diarrhea Virus N.D.
Bovine Parvovirus N.D.
Bluetongue Virus N.D.
Bovine Adenovirus N.D.
Rabies Virus N.D.Reovirus (Fluorescent Antibody) N.D.Infectious Bovine Rhinotracheitis (IBR) (Cytopathic Agents)
N.D.
Para Influenza 3 (PI3) (Hemadsorbing Agents)
N.D.
EMEA:CHMP/BWP7.3.2 Test for specified viruses7.3.3 BVDV7.3.4 Virus Neutralization Index
BVD Virus Type 1BVD Virus Type 2
N.D.N.D.A.R.
HORMONE METHOD RESULTS SPEC.Insulin EIA A.R.Progesterone EIA A.R.Estradiol EIA A.R.Testosterone EIA A.R.Thyroxine (T4) EIA A.R.Triiodothy-ronine (T3)
EIA A.R.
Cortisol EIA A.R.
A.R. = As ReportedN.D. = Not Detected
VIRAL SCREENHORMONE PANEL
STATEMENT OF ORIGINThis serum was derived from blood aseptically collected in an approved abattoir (single) in Australia. The country of origin of the animals is Australia. The serum was aseptically processed and filter steril-ized in Australia.
Product Fetal Bovine Serum - Sterile FilteredProduct Reference Number FBS1824-001Country of Origin AustraliaCertificate of Suitability On fileLot NumberFiltration Triple 0.1 MicronManufacture DateExpiration Date
Not For
Official
Use
COA-3
ANTIBODY METHOD RESULTS SPEC.BVD VNT A.R.IBR VNT A.R.PI3 ELISA A.R.BT ELISA A.R.Akabane ELISA A.R.EBL ELISA A.R.
A.R. = As ReportedN.D. = Not Detected
ANTIBIOTIC RESULTS SPEC.(Method: Liquid Chromatography - Mass Spectrometry - lower limit of detection 25.55 ng/mL)Chlortetracyline A.R.
Doxytetracyline A.R.
Oxytetracyine A.R.
Tetracyline A.R.
TEST METHOD RESULTS SPEC.pH 6.9-7.6
Osmolality Osmometer 280-365 mOsmol/kg
Total Protein Beckman Coulter Synchron Clinical Systems
3.0-4.5 g/dL
Albumin Electrophoresis A.R.Total Globulins
α1 Globulin β1 Globulinβ2 Globulinγ Globulin
Electrophoresis A.R.
Electrophoresis Pattern
Agarose Gel Plate
Typical
IgG ELISA ≤400 μg/mL
BIOLOGICAL PROFILE ANTIBODY PROFILE
SUBSTANCE RESULTS SPEC.(Method: Beckman DXC 800 Analyzer)
Sodium A.R.
Potassium A.R.
Chloride A.R.
Bicarbonate A.R.
Anion Gap A.R.
Glucose A.R.
Urea A.R.
Creatinine A.R.
Urea/Creatinine A.R.
Urate A.R.
Bilirubin total A.R.
Calcium A.R.
Phosphate A.R.
Alkaline Phosphatase A.R.
Gamma Glutamyl Transferase A.R.
Alanine Transaminase: (GPT) A.R.
Aspartate Transaminase: (GOT) A.R.
Lactate Dehydrogenase A.R.
Triglyceride A.R.
Iron A.R.
Iron Binding Capacity A.R.
Transferrin A.R.
Ferritin (Method: EIA) A.R.
Cholesterol
HDL LDL (Calculated) VLDL (Calculated)
≤1.2 mmol/LA.R.A.R.A.R.
BIOCHEMICAL PROFILE
FUNCTIONAL ASSAYS
TETRACYLINE SCREEN
S. SandersNucleus Quality Department
Date:
P. Shadle, PhDQuality Control Department
Date:
Not For
Official
Use
COA-4
For a digital copy, please visit https://www.nucleusbiologics.com
For a copy of the MSDS, please visit https://www.nucleusbiologics.com
Not For
Official
Use
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