The Comparative Hematology laboratory of KSVDL provides high quality services to practicing veterinarians, the Veterinary Health Center, researchers and industry. This is an AAVLD accredited laboratory.
- Iron and TIBC
- Ferritin Assay
- Non-heme Iron
- Feline Blood Card Typing
- Canine Blood Card Typing for DEA 1.1
The Comparative Hematology laboratory provides testing for iron and TIBC which is useful in the differential diagnosis of anemias and other iron disorders. Ferritin is another test used to estimate the total body stores of iron. Since the ferritin assay is a species specific test, we only offer it for canine, feline, elephant, equine, rhino, tapir, fur seal and dolphin. In addition to the serum testing we do for iron, TIBC, and ferritin, we provide a non-heme iron test performed on tissue. The non-heme iron test is used to determine body iron stores for diagnosing iron deficiencies or iron overload. Haptoglobin and ceruloplasmin are acute phase proteins that become elevated due to an acute phase reaction. We also offer testing for these proteins which are beneficial to determine infection, inflammation, malnutrition, or liver disease. The last two major tests we offer in the Comparative Hematology laboratory is blood typing for dogs and cats. Blood typing for an animal’s specific blood type is beneficial before a transfusion.
If you do not find a specific test listed, please contact Client Services at (785) 532-5650, toll free at 1-866-512-5650 or email@example.com for special testing submission and fees.
Iron in the body is a necessary metal required not only for the synthesis of hemoglobin but also for many cellular enzymes and coenzymes. Iron is transported in serum bound to the protein transferrin. Normally, only about one-third of the available binding sites on transferrin are occupied by iron. The total iron binding capacity is found in serum; therefore, it includes the amount of iron already bound to the transferrin (serum iron) plus the amount of iron required to saturate the unoccupied binding sites of transferrin. Clinically the determination of serum iron and total iron binding capacity is useful in the differential diagnosis of anemias and other iron disorders.
The spectrophotometric measurement of serum iron is accomplished by releasing the protein bound iron from its carrier protein transferrin and complexing the released iron with a suitable chromogen. In our method, the serum sample from any species is added to an acidic buffered reagent containing hydroxylamine, thiourea and Ferene.
Ferritin is the iron-apoferritin complex, which is one of the chief forms in which iron is stored in the body. In general, ferritin occurs in the gastrointestinal mucosa, liver, spleen, bone marrow, and reticuloendothelial cells.
This procedure is an enzyme-linked immunoabsorptive assay (ELISA) which measures serum ferritin by the sandwich technique. Serum ferritin is used to estimate the total body stores of iron. Values can also be increased with infections, cancer, and other acute phase reactions. The ferritin assay is species specific. At this time, we are limited to the ferritin assay for dog, cat, horse, rhino, tapir, fur seal, and dolphin.
Non-heme iron is iron not bound within a porphyrin ring.
This procedure measures tissue iron that is not bound to any heme containing compounds. It is used to determine body iron stores for diagnosing iron deficiencies or iron overload.
Haptoglobin is a plasma glycoprotein that binds ??-dimers of free hemoglobin. Its concentration in plasma differs in healthy individuals of various species and can change during disease. Most species have haptoglobin levels in the range of 100-300 mg/dL, but some species (i.e. cattle and pigs) normally have low plasma haptoglobin concentrations. Haptoglobin concentration decreases when free hemoglobin appears in plasma. That happens because haptoglobin-hemoglobin complexes are removed by the liver faster than haptoglobin can be synthesized. Haptoglobin synthesis increases during acute infection and inflammation as part of the acute phase reaction. Thus, serum haptoglobin concentration can be used to monitor the acute phase response. It is particularly valuable in those species that normally have low haptoglobin levels.
This method depends on the peroxidatic activity of hemoglobin and was adapted from the assay of Makimura and Suzuki. When hemoglobin is added in excess to serum samples, it binds to haptoglobin and becomes resistant to acid inactivation. In contrast, the peroxidatic activity of free hemoglobin is lost. The haptoglobin concentration is calculated with a standard curve prepared by incubating known amounts of hemoglobin with a serum sample containing a haptoglobin concentration greater than 150 mg/dL.
Ceruloplasmin is an “acute reactive” protein and its concentration in serum is moderately increased (50 to 100 percent) in conditions of physiological stress. Increased levels of the protein are encountered in acute infections, in chronic conditions such as rheumatoid arthritis, lupus, and cirrhosis, after myocardial infarctions, (tissue necrosis), and after stress of surgery. Somewhat greater elevations (up to two-fold) are observed in hepatitis, Hodgkins disease, metastatic carcinoma, and hyperthyroidism. Diminished levels of the enzyme are encountered in several conditions: nutritional protein deficiency (malabsorption as well as malnutrition), severe liver disease, and nephrosis. About 94 to 95 percent of the total copper in plasma is present in the ceruloplasmin molecule, and the remainder is bound to albumin; only a trace is present as free Cu2+. By virtue of its copper content, ceruloplasmin is an important vehicle for transport of copper in the body.
This method depends on the oxidative activity of p-phenylenediamine. When this substrate is combined with serum, it produces a purple-colored compound and is read colorometrically.
Cat blood typing is used to determine the cat’s specific blood type before a transfusion. An animal is transfused with type specific blood to prevent a transfusion reaction. Transfusion reactions can cause serious illness or death. Cats have three blood types (A, B, and AB). Most cats (>99%) are blood type A. Type B cats have a natural occurring antibody to blood type A. Some purebred breeds have a high incidence of blood type B (17-59%). When cats with type B are transfused with type A RBCs, an acute transfusion reaction can occur.
This procedure is performed on a specially designed blood typing card manufactured exclusively in our laboratory. Presence or absence of agglutination in the test wells of the card determine blood type, A, B, or AB.
Dog blood typing is used to determine the dog’s specific blood type before a transfusion. An animal is transfused with type specific blood to prevent a transfusion reaction. Transfusion reactions can cause serious illness or death. Dogs have at least 7 blood types. Blood types DEA (dog erythrocyte antigen) 1.1 and 1.2 are the most immunogenic and when transfused into a dog without those blood types will alloimmunize the transfused dog. Some dogs have a naturally occurring antibody to blood type 7. The “universal donor” should be negative for blood types 1.1, 1.2, and 7 and negative for antibody to blood type 7.
This procedure is performed on a specially designed blood typing card manufactured exclusively in our laboratory. Presence or absence of agglutination in the test wells of the card determine blood type DEA 1.1 positive or negative.