The largest database of trusted experimental protocols

18 protocols using vet scan analyzer

1

Coagulation, Inflammation, and Hematology

Check if the same lab product or an alternative is used in the 5 most similar protocols
Blood was collected at scheduled time points (Days −7, 0, 3, 5, 7, 9, 11, 13, and 14, relative to exposure). Coagulation times were determined on whole blood collected with no additives, using an IDEXX Coag Dx Analyzer (IDEXX Laboratories, Westbrook, ME, USA). These blood samples were processed to obtain the serum. Serum was analyzed to measure C-reactive protein (CRP) levels using a Piccolo BioChemistry Panel Plus on a Vet Scan analyzer (Abaxis, Inc., Union City, CA, USA). Whole blood was also collected into tubes containing ethylenediaminetetraacetic acid (EDTA) for complete blood counts (CBC) using a Procyte Dx Hematology Analyzer (IDEXX laboratories, Westbrook, ME, USA) and for clinical chemistry using the mammalian liver enzyme profile rotor on a Vet Scan analyzer (Abaxis, Inc., Union City, CA, USA).
+ Open protocol
+ Expand
2

Measuring Serum AGEs in Animal Studies

Check if the same lab product or an alternative is used in the 5 most similar protocols
The serum samples obtained from the blood of the experimental animals were stored in sterile tubes at −80 °C until analysis. Blood urea nitrogen (BUN) and serum creatinine (SCr) concentrations were analyzed using a Vet Scan analyzer (Abaxis, Inc., Union City, CA, USA).
The OxiSelectTM AGEs Competitive ELISA Kit from Cell Biolabs (San Diego, CA, USA) was used to determine the concentrations of AGEs in the serum. The circulating AGEs were analyzed depending on the sample’s fluorescence or absorbance in each well, as measured using a fluorescence microplate reader (Molecular Devices, San Jose, CA, USA) at 450 nm.
+ Open protocol
+ Expand
3

Hematology and Clinical Chemistry Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Post-challenge time points for blood sampling and rectal temperature measurements varied by study and are listed in the supplementary table legends. The following hematology and clinical chemistry parameters are shown in the supplementary tables: granulocyte counts, levels of alanine aminotransferase, prothrombin time (PT), and activated partial thromboplastin time (aPTT). Granulocyte counts were determined in blood containing EDTA using either a VetScan HM2 Analyzer (Abaxis Inc,) or a COULTER Ac.T 5diff AL (Beckman Coulter Inc.). Clinical chemistry parameters were measured in serum using a VetScan analyzer or Piccolo Xpress (both Abaxis Inc). PT and aPTT were measured in a Coag DX analyzer (IDEXX Laboratories Inc.). Petechial rash was recorded on clinical observation sheets at least twice daily by staff blinded to study treatment.
+ Open protocol
+ Expand
4

Serum Enzyme Analysis Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
Serum samples were aliquoted into sterile tubes and frozen at -80°C within 2 h of collection for subsequent analysis. The activities of AST, ALT, ALP, and r-glutamyl transferase (r-GTP) were analyzed by using a VetScan analyzer (Abaxis, Inc., Union City, CA).
+ Open protocol
+ Expand
5

Determination of Hepatic Glutathione Levels

Check if the same lab product or an alternative is used in the 5 most similar protocols
A portion of the liver tissue was washed with cold PBS containing 0.16 mg/mL heparin to prevent coagulation. Total glutathione (GSH) content was measured by using an assay kit in accordance with manufacturer instructions (Enzo Life Sciences (NY, USA). Tissue samples (100 mg) were homogenized in ice-cold 5% (w/v) meta-phosphoric acid and centrifuged at 12,000 g for 10 min at 4°C. The reaction mixture was added to the diluted samples (10 µL) and measured using a VetScan analyzer (Abaxis, Union City, CA). Total GSH was expressed as nmol/mg protein and quantitated using a standard curve.
+ Open protocol
+ Expand
6

Comprehensive Blood Analysis in Animal Studies

Check if the same lab product or an alternative is used in the 5 most similar protocols
Blood was collected from sedated animals at scheduled time points, as described in Section 2.2 and Figure 1a. Coagulation analysis, complete blood counts (CBC), and clinical chemistry analyses were performed, as previously described [38 (link),39 (link),40 (link),41 (link)]. Serum was also analyzed for C-Reactive Protein (CRP) levels using a Piccolo BioChemistry Panel Plus on a Vet Scan analyzer (Abaxis, Inc., Union City, CA, USA). Hematology and serum chemistry parameters shown below (Table 1) are provided (Figure 1c–h). The coagulation assessments performed were activated partial thromboplastin time (aPTT) and prothrombin time (PT) (Figure 1i,j).
+ Open protocol
+ Expand
7

Liver Enzyme and Hematology Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Biochemical analysis was performed using the mammalian liver enzyme profile rotor on a Vet Scan analyzer (Abaxis, Inc., Union City, CA, USA). Coagulation times were determined using the IDEXX Coag Dx Analyzer (IDEXX Laboratories, Westbrook, ME, USA). Vetscan HM2 hematology analyzer (Abaxis, Inc., Union City, CA, USA) (IACUC 1381) or a Procyte Dx Hematology Analyzer (IDEXX laboratories, Westbrook, ME, USA) (IACUCs 1532 and 1529) was used to obtain neutrophil, lymphocyte, and red blood cell counts.
+ Open protocol
+ Expand
8

Comprehensive Blood and Urine Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Blood was collected from the abdominal aorta and collected in 15-mL plain tubes and lavender-top (EDTA) specimen tubes for analysis of hemoglobin A1C (HbA1C). Within 1 h of collection, plain tube blood samples were then centrifuged at 3000 rpm for 10 min to collect serum. The sera were immediately stored at −80 °C to analyze blood urea nitrogen (BUN), serum creatine (sCr), glucose levels, aspartate aminotransferase (AST), and alanine aminotransferase (ALT) activities, by using an Olympus AU400 chemistry analyzer (Tokyo, Japan). Advanced glycation end products (AGEs) using the VetScan analyzer (Abaxis Inc., Union City, CA, USA). The levels of urinary albumin, creatinine, and protein were estimated by using a Hitachi 7180 auto analyzer (Hitachi, Tokyo, Japan).
+ Open protocol
+ Expand
9

Liver Histopathology and Damage Markers

Check if the same lab product or an alternative is used in the 5 most similar protocols
Liver ceria content was estimated by induction coupled plasma-mass spectrometry (ICP-MS) as described elsewhere [18 (link)]. In other experiments, portions of each liver were formalin fixed, sectioned, and stained with hematoxylin and eosin (H&E) for histopathological examination. Microscopic images were captured using an EVOS XL Core microscope (Fisher Scientific, Pittsburgh, PA, USA). Liver damage markers in the serum were estimated using an Abaxis VetScan analyzer (Abaxis, UnionCity, CA) and Myriad RBM (Austin, TX).
+ Open protocol
+ Expand
10

Comprehensive Primate Blood Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Whole blood was collected at pre-determined study days 7, 0, 3, 4, 5, 6, at scheduled euthanasia, and at moribund euthanasia. Whole blood was collected into tubes containing Ethylenediaminetetraacetic acid (EDTA) for Complete blood Counts (CBC) analysis and clinical chemistry. CBC was performed using a Procyte Dx Hematology Analyzer (IDEXX laboratories, Westbrook, Maine, USA) and the parameters analyzed included white blood cell counts, neutrophil counts and percent, lymphocytes counts and percent, monocytes counts and percent, red blood cell counts, percent hematocrit, reticulocyte counts and percent, platelet counts, and percent platelet. Clinical chemistry was performed using the mammalian liver enzyme profile rotor on a Vet Scan analyzer (Abaxis, Inc., Union City, CA, USA). Coagulation times were determined on whole blood with no additives using an IDEXX Coag Dx Analyzer (IDEXX Laboratories, Westbrook, Maine, USA). Parameters were evaluated against reference ranges established by Texas Biomed clinical pathology derived from a cohort of clinically healthy macaques.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!