Animal serum Fetal / Newborn / Calf / Adult Bovine serum

Example Specifications

Product description

Fetal / Newborn / Calf / Adult Bovine serum, sterile filtered

Source

Material was collected from healthy animals at a MAF inspected establishment, NZL

Volume

10L – 100L

Apperance

Liquid

Storage

Keep frozen at -20°C or colder

Specifications

Analytes Results
Mycoplasma Negative
Endotoxin <0.5 EU/mL
Total Protein 2 – 6 g/dL
pH 7.8
Osmolality 258 mOsm/kg
Sterility<USP 71> No Growth

Biochemical (Beckman DXC 800 Analyser)

Biochemical Results
Sodium 137 mmol/L
Potassium 5.4 mmol/L
Chloride 101 mmol/L
Bicarbonate 25 mmol/L
Anion gap 11 mmol/L
Glucose 5.5 mmol/L
Urea 5.1 mmol/L
Creatinine 67 umol/L
Urea/Creatinine ratio 76
Urate 0.03 mmol/L
Bilirubin total 6 umol/L
Calcium 2.6 mmol/L
Phosphate 2.36 mmol/L
Alkaline Phosphatase 181 U/L
Gamma Glutamyl Transferase 632 U/L
Alanine Transaminase 15 U/L
Aspartate Transaminase 69 U/L
Lactate Dehydrogenase 639 U/L
Triglyceride 0.3 mmol/L
Cholesterol

Test Results

Test Results Spec
Visual Examination -(Visual) Satisfactory Satisfactory
Sterility (Broth Culture 14 day incubation) Sterile after 14 days in Thiogly-collate and in Tryptic Broth Sterile
Mycoplasma -(broth Culture day Incubation) Not Detected Not Detected
Bovine Viral Diarrhea Virus (Fluorescent Antibody) Not Detected Not Detected
Infectious Bovine Rhinotracheitis (IBR) (Cytopathic Agents) Not Detected Not Detected
Para Influenza 3(PI3) (Haemadsorbing Agents) Not Detected Not Detected
Cytopathic effects Not Detected Not Detected
pH 8.0 6.9-8.1
Osmolality (Osmometer) 285 240-340
Total Protein (Beckman Coulter SynchronClinical Systems) 63 % ≥ 35
Albumin (Electrophoresis) 40
Total Globulins (Electrophoresis): Alpha 1 15 %
Alpha 2 5 %
Beta 16 %
Gamma 24 %
Electrophoresis pattern (Agarose Gel Plate) Typical Typical
Haemoglobin (UV/VIS Spectrophotometer) 0.095 g/ml < 0.2
Endotoxin (Kinetic Turbidimetric) < 1 ≤30

This product is for further manufacturing or research and development use only. Neither product reliability after removal from original container and/or treatment of product whatsoever, nor any responsibility for misuse of product can be granted. Post market surveillance and vigilance is the receiver's duty only.

Specifications are customizable. Vial fill size, form, concentrations, markers, volume and number of levels.