ERCC2 FISH Probe-核酸检测-试剂-生物在线
ERCC2 FISH Probe

ERCC2 FISH Probe

商家询价

产品名称： ERCC2 FISH Probe

英文名称： ERCC2 FISH Probe

产品编号： FA0420

产品价格： 0

产品产地： 台湾

品牌商标： Abnova

更新时间： null

使用范围： null

亚诺法生技股份有限公司（Abnova)
  • 联系人 :
  • 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
  • 邮编 : 11493
  • 所在区域 : 台湾
  • 电话 : +886-920**1152
  • 传真 : +886-2-8751-1186
  • 邮箱 : sales@abnova.com.tw
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  • Specification
  • Product Description:
  • Made to order FISH probes for identification of gene amplification using Fluorescent In Situ Hybridization Technique. (Technology)
  • Storage Instruction:
  • Store at 4°C in the dark.
  • Supplied Product:
  • DAPI Counterstain (1500 ng/mL ) 250 uL
  • Origin:
  • Human
  • Source:
  • Genomic DNA
  • Notice:
  • We strongly recommend the customer to use FFPE FISH PreTreatment Kit 1 (Catalog #: KA2375 or KA2691) for the pretreatment of Formalin-Fixed Paraffin-Embedded (FFPE) tissue sections.
  • Regulation Status:
  • For research use only (RUO)
  • Applications
  • Application Image
  • Fluorescent In Situ Hybridization (Cell)
  • Gene Information
  • Entrez GeneID:
  • 2068
  • Gene Name:
  • ERCC2
  • Gene Alias:
  • COFS2,EM9,MGC102762,MGC126218,MGC126219,TTD,XPD
  • Gene Description:
  • excision repair cross-complementing rodent repair deficiency, complementation group 2
  • Gene Summary:
  • The nucleotide excision repair pathway is a mechanism to repair damage to DNA. The protein encoded by this gene is involved in transcription-coupled nucleotide excision repair and is an integral member of the basal transcription factor BTF2/TFIIH complex. The gene product has ATP-dependent DNA helicase activity and belongs to the RAD3/XPD subfamily of helicases. Defects in this gene can result in three different disorders, the cancer-prone syndrome xeroderma pigmentosum complementation group D, trichothiodystrophy, and Cockayne syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq
  • Other Designations:
  • excision repair cross-complementing rodent repair deficiency, complementation group 2 protein,xeroderma pigmentosum complementary group D
  • Related Disease

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