Access Bio MCH-N10081 说明书

世界*实验材料供应商 Access Bio上海金畔生物为其中国代理, Access Bio在一直是行业的*,一直为广大科研客户提供zui为的产品和服务,上海金畔生物一直秉承为中国科研客户带来的产品,的服务, Access Bio就是为了给广大科研客户带来更加完善的产品和服务,您的满意将是我们zui大的收获

Access Bio中国代理Access Bio上海代理, Access Bio北京代理,Access Bio广东代理, Access Bio江苏代理Access Bio湖北代理,Access Bio天津,Access Bio黑龙江代理,Access Bio内蒙古代理,Access Bio吉林代理,Access Bio福建代理, Access Bio江苏代理, Access Bio浙江代理, Access Bio四川代理,

 

Access Bio 通过研究、开发和制造体外快速诊断试验、生物传感器和分子诊断产品,Access致力于预防和早期诊断传染病。早期准确诊断是有效治疗的关键。我们的核心的体外诊断技术包括化学、生化和分子生物学产品。访问生物努力建立一个基础,为所有人的福祉。

访问生物试图满足市场需求的准确和成本效益的体外诊断在一个全新的技术和产品开发水平。我们本着“为客户提供物美价廉的产品,永续经营”的宗旨,以此为宗旨,为世界各地的客户服务。

 

CareStart™ CAH*

Specifications

  • Test TypeMolecular diagnostic test
  • SpecimenBlood sample
  • Result Time8 Hours (including DNA extraction time)
  • Package Size100 tests/box

CAH

Congenital Adrenal Hyperplasia (CAH) is a genetic disorder that limits adrenal glands’ ability to produce certain vital hormones, causing altered development of primary or secondary sex characteristics in affected infants and children, or adults. It can be fully treated when detected early through newborn screening with high sensitive molecular diagnostic tests.

Features & Benefits

  • Screening for congenital adrenal hyperplasia (CAH) mutations on CYP21, using allele-specific primer extension (ASPE) and bead-array hybridization.
  • Detection of the 10 major point mutations and the 8 bp deletion at Chromosome 6p21.3
  • Detection of a large deletion between CYP21A1p and CYP21A2
  • Semi-quantitative test with bead array for point mutation and agarose electrophoresis for a large deletion
  • Approximay 8hours from DNA extraction to data reporting.

Allele-specific detection

(Amplified target DNAs with different sizes)

Product Cat. No. Package Size
CareStart™ CAH MCH-N10081 100 tests/box