GGP Bovine 150K

Bovine-GGP HD 150K

SKU N°  11  |  Numéro de catalogue 

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.
$103.00 chacune
Quantité minimale requise : 1
Pour cet article, la quantité commandée doit être un multiple d’une boîte. Quantité par boîte : 1

Our highest density genomic profiler, the GGP Bovine 150K is designed to provide the most comprehensive data to researchers and producers alike. Using the active genes plus denser coverage provides more power to predict cattle and progeny performance. The GGP Bovine 150K offers exclusive content on thousands of “causative” markers tied to issues such as embryonic or fetal death as well as abnormalities that interfere with normal cattle growth development, and gain.

Tests supplémentaires

Des tests supplémentaires peuvent être ajoutés à l’étape suivante lors du téléchargement de votre formulaire de demande.
Spécifications
MarqueGeneSeek® Genomic Profiler™
Races prises en chargeAll breeds supported
EspèceBovin, Bœuf, Produits laitiers
Résultats des donnéesGGP 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.
Informations sur la soumissionProducers 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.
Conditions génétiquesBVDV, Arthrogryposis Multiplex (AM), Arachnodactylie contractuelle (« Contractural Arachnodactyly », CA), Chondrodysplasie (CHO), Couleur de robe, Malformation vertébrale complexe (MVC), Duplication du développement (DD), Dilueur (DL) de couleur de robe, Couleur de robe Dun (DN), À corne/sans corne (« Horned/Polled », HP), Hypotrichose (HY), Épilepsie idiopathique (IE), Alpha Mannosidose (MA), Maladie des urines à odeur de sirop d'érable (« Maple Syrup Urine Disease », MSUD), Myostatine (MYO), Hydrocéphalie neuropathique (HN), Ostéopétrose (OS), Hypoplasie Pulmonaire Anasarca (« Pulmonary Hypoplasia Anasarca », PHA), Hémimélie tibiale (« Tibial Hemimelia », TH), Hypopigmentation oculocatanée (HO), BLAD, Brachyspina, DUMPS, Caséine kappa, Leptine, Tendreté, Pompes, CMS, Lait de poisson

Documents

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