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Merck

11093657910

Roche

DIG DNA标记和检测试剂盒

greener alternative

别名:

Dna 标记和检测试剂盒,dig

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25 REACTIONS
$1,700.00

$1,700.00


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选择尺寸

变更视图
25 REACTIONS
$1,700.00

About This Item

分類程式碼代碼:
41105500

$1,700.00


请联系客服了解存货情况

用途

sufficient for 25 labeling reactions
sufficient for 50 blots

品質等級

製造商/商標名

Roche

環保替代產品特色

Designing Safer Chemicals
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

環保替代類別

儲存溫度

−20°C

一般說明

DIG DNA标记和检测试剂盒是使用便捷的试剂盒,用地高辛-脱氧尿苷三磷酸(dUTP)标记DNA随机引物,通过酶免疫法对杂交产物进行碱解,测定颜色。在此方法中,使用随机寡核苷酸3′-OH末端用作引物,在Klenow聚合酶的作用下合成变性 DNA 的互补 DNA 链。

内容物:
  • 未标记的对照DNA 1, 100 μg/ml
  • 未标记的对照DNA 2, 200 μg/ml
  • DNA稀释缓冲液
  • DIG标记的对照DNA, 5.2 μg/ml
  • 10X 六核苷酸混合物
  • 10x dNTP标记混合物
  • Klenow 酶,标记等级,2 U/μl
  • 抗地高辛-AP结合物,750 U / ml
  • NBT/BCIP 浓缩储存液
  • 封闭剂
我们致力于为您提供更环保的替代产品,以符合“绿色化学的12项原则”的一项或多项原则要求。本产品为一种安全的化学品。DIG系统是灵敏且具有成本效益的方案,可替代核酸的放射性标记和检测方法。有许多已发表论文证明了DIG系统的通用性,因此,使用放射性标记不再是标记用于杂交的DNA的唯一选择。

特異性

灵敏度和特异性:1 μg模板37℃,1小时培育,标准标记反应会产生260ngDIG-标记DNA,20小时培育会生成780ng。DIG检测灵敏度取决于杂交反应中DIG-标记探针浓度和颜色反应持续时间。

應用

DIG DNA标记和检测试剂盒已用于多种杂交技术:
  • Southern 印迹[1][1]
  • Northern 印迹[2]
  • 斑点印迹
  • 菌落和噬菌斑筛查
用抗DIG-碱性磷酸酶偶联物、底物NBT(硝基蓝四唑盐)和BCIP(5-溴-4-氯-3-吲哚基磷酸盐,甲苯铵盐)检测DIG标记的杂交产物。

包裝

1个试剂盒包含10种组分。

準備報告

工作浓度:将抗体稀释到1:5000

其他說明

仅用于生命科学研究。不可用于诊断。

仅试剂盒组分

产品编号
说明

  • Unlabeled Control DNA 1 100 µg/ml

  • Unlabeled Control DNA 2 200 µg/ml

  • DNA Dilution Buffer

  • DIG-labeled Control DNA 5.2 µg/ml

  • Hexanucleotide Mix 10x concentrated

  • dNTP Labeling Mixture 10x concentrated

  • Klenow Enzyme, Labeling grade 2 U/µl

  • Anti-digoxigenin-AP-conjugate antibody 750 U/ml

  • NBT/BCIP Concentrated Stock Solution

  • Blocking Reagent

查看所有结果 (10)

儲存類別代碼

13 - Non Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

does not flashNot applicable

閃點(°C)

does not flashNot applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Shun Sawatsubashi et al.
Scientific reports, 8(1), 593-593 (2018-01-14)
CRISPR/Cas9-based genome editing has dramatically accelerated genome engineering. An important aspect of genome engineering is efficient knock-in technology. For improved knock-in efficiency, the non-homologous end joining (NHEJ) repair pathway has been used over the homology-dependent repair pathway, but there remains
Jiaqiang Wang et al.
Cell, 175(7), 1887-1901 (2018-12-15)
In early mammalian embryos, it remains unclear how the first cell fate bias is initially triggered and amplified toward cell fate segregation. Here, we report that a long noncoding RNA, LincGET, is transiently and asymmetrically expressed in the nucleus of
Diana C Garcia-Ramon et al.
Microbial biotechnology, 11(2), 302-316 (2017-10-14)
Bacillus pumilus strain 15.1 was previously found to cause larval mortality in the Med-fly Ceratitis capitata and was shown to produce crystals in association with the spore. As parasporal crystals are well-known as invertebrate-active toxins in entomopathogenic bacteria such as
Nasser Shakhssalim et al.
Cancer cell international, 13(1), 120-120 (2013-12-07)
Bladder cancer is a relatively common and potentially life-threatening neoplasm that ranks ninth in terms of worldwide cancer incidence. The aim of this study was to determine deletions and sequence variations in the mitochondrial displacement loop (D-loop) region from the
Hongshun Li et al.
International journal of molecular sciences, 22(11) (2021-06-03)
The vegetative phase transition is a prerequisite for flowering in angiosperm plants. Mulberry miR156 has been confirmed to be a crucial factor in the vegetative phase transition in Arabidopsis thaliana. The over-expression of miR156 in transgenic Populus × canadensis dramatically

商品

Digoxigenin (DIG) labeling methods and kits for DNA and RNA DIG probes, random primed DNA labeling, nick translation labeling, 5’ and 3’ oligonucleotide end-labeling.

地高辛(DIG)标记方法和试剂盒适用于DNA和RNA DIG探针、随机引物DNA标记、切口平移标记、5'和3'寡核苷酸末端标记。

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

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