GGP Bovine 150K
Bovine-GGP HD 150K
Nº de SKU 11 | Número de catálogo
Neogen’s GGP Bovine 150K is an ideal cattle DNA testing solution for elite seedstock, donor dams, A.I. studs and high-impact cattle. Key features of the GGP Bovine 150K include:
- Smart design. SNPs specifically chosen for high minor allele frequency and uniform coverage of the genome for most beef and dairy breeds of cattle.
- Comprehensive information. Includes impactful new markers for cattle performance and reproduction.
- Parentage Verification. Includes all commonly utilized USDA and ISAG parentage markers.
Teste adicional
Coat Color Dilutor (DL)
This dilution gene causes black coat color to be gray and red coat color to be yellow in the Hereford, Simmental and Gelbvieh breed.
Dun Coat Color (DN)
This dilution gene causes black coat color to be diluted to shades of dark brown to golden. Red pigment is not diluted by this mutation.
Kappa Casein
Leptin
Tenderness
Holstein Cholesterol Deficiency
Deficiency of Uridine Monophosphate Synthase (DUMPS)
Bovine Lueukocyte Adhesion Deficiency (BLAD)
Brachyspina
Pompes (E7, E13, E18)
Maple Syrup Urine Disease (MSUD)
Causes mental and physical retardation, feeding problems, and a maple syrup odor to the urine.
Fish Milk
Metabolism error associated with a fishy off-flavor in cow’s millk due to elevated levels of trimethylamine
Tibial Hemimelia (TH)
Affected animals are born with severe deformities including twisted rear legs with fused joints, large abdominal hernias and/or skull deformities.
Oculocutaneous Hypopigmentation (OH)
Affected animals are known to have eyes with irises that are pale blue around the pupil.
Neuropathic Hydrocephalus (NH)
More commonly known as "waterhead", affected animals are born dead with an extremely large head with little or no brain material or spinal cord.
Osteopetrosis (OS)
Also known as “marble bone”, affected animals phenotypically possess a short lower jaw and impacted molars as well as elongated, fragile bones that are easily broken.
Pulmonary Hypoplasia Anasarca (PHA)
Affected animals are stillborn due to underdeveloped lungs and swelling caused by excessive fluid retention.
Myostatin (MYO)
Most commonly referred to as “double muscling”. Possible variants tested include C313Y, nt419, E226X, nt821, E291X, Q204X, D182N, F94L, and S105C.
Alpha Mannosidosis (MA)
Affected animals develop poor coordination and an aggressive disposition when disturbed.
SeekSire™ Parentage
SeekSire™ parentage testing compares DNA markers from bulls (or cows) with DNA from calves to verify the calves’ parentage.
Horned/Polled (HP)
Hypotrichosis (HY)
Also known as "hairlessness", affected animals have partial or total hair loss.
Idiopathic Epilepsy (IE)
Also referred to as “shaker calf”, affected animals are prone to seizures.
Developmental Duplication (DD)
Affected animals are born with all, or part of, an extra limb.
Complex Vertebral Malformation (CVM)
Complex Vertebral Malformation (CVM) is a lethal hereditary syndrome in Holstein animals causing malformed calves that are aborted or die shortly after birth.
Contractural Arachnodactyly (CA)
Also known as “fawn calf”, CA results in an abnormality of skeletal development in Angus cattle.
Arthrogryposis Multiplex (AM)
Known as "curly calf", affected animals (those with two copies of the recessive allele) are stillborn and have a twisted or curved spine and extended and contracted limbs.
Bovine Viral Diarrhea Virus - Persistently Infected (BVDV-PI)
Neogen® offers fast and accurate testing for the detection of Bovine Viral Diarrhea Virus (BVDV).
| Especificações | ||
|---|---|---|
| Marca | GeneSeek® Genomic Profiler™ | |
| Raças compatíveis | All breeds supported | |
| Espécies | Bovinos, Gato, Douglas Fir | |
| Resultados de dados | GGP Bovine 150K provides raw genotype information back to industry partners for use in a formal genetic evaluation. Parentage analysis can be performed by Neogen, if desired. | |
| Informações sobre o envio | Producers may purchase GGP Bovine 150K through one of Neogen’s partner breed associations or their genetic evaluation provider. If interested in the product for research purposes, please contact Neogen directly. | |
| Doenças genéticas | BVDV, Artrogripose múltipla (AM), Contratura aracnodactilia (CA), Condrodisplasia (CHO), Cor da pelagem, Complexo da Malformação Vertebral (CVM), Duplicação no desenvolvimento (DD), Diluidor da cor da pelagem (DL), Cor de pelagem parda (DN), Chifres (HP), Hipotricose (HY), Epilepsia idiopática (IE), Alfa-manosidose (MA), Doença do xarope de bordo na urina, Miostatina (MYO), Hidrocefalia neuropática (NH), Osteopetrose (OS), Hiipoplasia pulmonar anasarca (PHA), Hemimelia tibial (TH), Hipopigmentação óculo-cutânea (OH), BLAD, Brachyspina, ATERROS, K-caseína, Leptina, Sensibilidade, Pompe, CMS, Chanos-Chanos (peixe-leite) | |
Documentos
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Treinamento
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