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ApexBio/ApexPrep DNA Plasmid Miniprep Kit/300 tests/A5001

价格
¥4000.00
货号:A5001
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品牌:ApexBio
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  • ApexPrep DNA Plasmid Miniprep Column Only
ApexPrep DNA Plasmid Miniprep Kitused for isolation of plasmid DNA

Catalog No.A5001
SizePriceStockQty
50 tests
$40.00
In stock
300 tests
$200.00
In stock

Tel: +1-832-696-8203

Email: sales@apexbt.com

Worldwide Distributors

Sample solution is provided at 25 µL, 10mM.

Product Citations

1. Wang EX, Ding MZ, et al. "Reorganization of a syntheticmicrobial consortium for one-step vitamin C fermentation." Microb Cell Fact. 2016 Jan 25;15:21.PMID:26809519

Description

For purification ofup to 20 μg molecular biology grade plasmid DNA

  • Ready-to-use plasmid DNA in minutes
  • Reproducible yields of molecular biology grade plasmid DNA
  • Single protocol for high- and low-copy vectors

The ApexPrep Spin Miniprep Kit is designed for isolation of up to 20 μg high-purity plasmid or cosmid DNA for use in routine molecular biology applications such as fluorescent and radioactive sequencing and cloning.

DNA Miniprep Protocol Using a Microcentrifuge1. Inoculate 1-5 ml LB medium (selective antibiotic added) with a single colony, incubate with vigorous shaking at 37 °C overnight. 2. Harvest bacteria by centrifuging at > 6000 rpm for 5 min. Remove supernatant and keep pellet. 3. Resuspend bacterial pellet with 250 μl Buffer P1 and transfer to a fresh microcentrifuge tube. 4. Add 250 μl Buffer P2 and mix gently by inverting 5-6 times at room temperature. 5. Add 350 μl Buffer P3 and mix gently by inverting 5-6 times. Spin down at 12000 rpm for 10 min to remove bacterial/protein debris. Transfer supernatant to a spin column. 6. Centrifugation at 6000 rpm for 1 min. Discard flow-through.7. (Optional), wash spin column with 0.5 ml Buffer PB; centrifuge at 6000 rpm for 1 min, and discard flow-through.8. Wash spin column with 0.75 ml Buffer PE; centrifuge at 6000 rpm for 1 min, and discard flow-through.9. Centrifuge at 12000 rpm for an additional 1 min to remove residual wash buffer.10. To elute DNA, place the column in a clean 1.5 ml collection tube. Add 50 μl Buffer EB to the center of the membrane, let stand for 1 min, and centrifuge at 12000 rpm for 1 min to collect eluted DNA.

ApexBio的3X FLAG Peptide FLAG标签系统利用与目标蛋白质1融合的短而亲水的8个氨基酸的肽段。FLAG肽与抗体M1结合。结合是钙依赖性方式2还是非依赖性3仍存在争议。该系统的缺点是单克隆抗体纯化基质不如其他基质稳定。通常,可以用特异性单克隆抗体检测小标签。为了改善对FLAG标签的检测,已经开发了3x FLAG系统。这种三级FLAG表位是亲水的,长22个氨基酸,可以检测到高达10 fmol的表达融合蛋白。激烈热球菌的带有FLAG标签的麦芽糖糊精结合蛋白已被结晶4,其晶体质量与未标记蛋白的晶体质量非常相似。 最后,可以通过用肠激酶处理去除FLAG标签,肠激酶对肽序列5的5个C末端氨基酸具有特异性。