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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
运输过程中保存:2-8℃
- 保质期:
1年
- 英文名:
EZElisa™ Xeroderma Pigmentosum, Complementation Group D (XPD) Kit
- 库存:
100
- 供应商:
艾美捷科技
EZElisa™着色性干皮病,补体D组(XPD)试剂盒,EZElisa™ Xeroderma Pigmentosum, Complementation Group D (XPD) Kit,着色性干皮病,补体D组(XPD)试剂盒, Xeroderma Pigmentosum, Complementation Group D (XPD) Kit
产品名称:EZElisa™黄嘌呤脱氢酶(XDH)试剂盒-EZElisa™ Xeroderma Pigmentosum, Complementation Group D (XPD) Kit
产品货号:A-QEK01568-96wells
产品规格:96wells

Enzyme Immunoassay for the estimation of EZElisa™ Xeroderma Pigmentosum, Complementation Group D (XPD) in serum and plasma, tissue homogenates and other biological fluids.
种属:Human
检测方法:比色法
检测范围:0.156 - 10 ng/ml

该EZElisa™着色性干皮病,补体D组(XPD)试剂盒ELISA的特点包括:即用即用的操作步骤标准化和高重复性批次之间的一致性准确性和精确性经过七个点的验证,符合金环标准质量ELISA的要求,这是Biogradetech质量的基准标志。EZElisa™ ELISA试剂盒用于评估样品中的特定生物标志物,样品可以是血清

运输过程中保存:2-8℃
点击:EZElisa™黄嘌呤脱氢酶(XDH)试剂盒-EZElisa™ Xeroderma Pigmentosum, Complementation Group D (XPD) Kit更多Biogradetech产品信息价格,货期,产品说明,百度搜“艾美捷科技”进入官网网站,查看具体产品且快速下单。

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文献和实验Complementation Assays Adapted for DNA Repair-Deficient Keratinocytes
autosomal syndromes xeroderma pigmentosum (XP), Cockayne syndrome (CS), or trichothiodystrophy (TTD). Classical approaches such as somatic cell fusions or microinjection assays have formalized the genetic complexity of these related but clinically distinct
Nucleotide Excision Repair Assay in Drosophila melanogaster Using Established Cell Lines
by genetic analyses of mainly human, rodent, and yeast repairdeficient mutants (1 ,2 ). In particular, cultured cells derived from patients with xeroderma pigmentosum (XP), a human autosomal-recessive disease causing defects in NER, as well as from rodent
Dual-Incision Assays for Nucleotide Excision Repair Using DNA with a Lesion at a Specific Site
strand on the 5′- and 3′-sides of a lesion (1 ). In humans, defects in the genes that participate in NER can lead to a rare recessive disorder, xeroderma pigmentosum (XP). Hypersensitivity to sunlight and a predisposition to skin cancer
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