LApro Taq DNA Polymerase(E00013)
- 供应商
- 北京华夏远洋科技有限公司
- 认证
- 性状
- 试剂
- 适应症
- 科研试验
- 联系电话
- 010-62898668
- 手机号
- 15201195988
- 联系人
- 朱少雄
- 所在地
- 北京市丰台区造甲街110号2号平房(新村企业集中办公区)
laprota是具有5"→3"dna聚合活性和3"→5"校对活性的dna聚合酶,可用于高效扩增长片段的复杂模板。laprota在75℃(其反应适温度)时,扩增产物的率是普通ta的10倍以上,可扩增长达17.5kb来自于人genomicdna或来自于λdna的长达20kb的dna片段。使用laprota扩增长片段dna模板时,可有效减少拖尾效应,去除背景影响,扩增产物有3"端有一个a碱基,可以直接用于t/a克隆。
dna polymerase
1.5ml×2 2x buffer,500mm tris-hcl (ph8.9, 25℃),0.5% tween 20,0.5%nonidet p40,1mg/ml bsa,3mm mgcl2
高保真pcr扩增,错配率只有2×10-6。没有5"→3"外切酶活性和3"→5"校对活性,具有ta克隆所需的extendase活性。
1单位(u)dna polymerase活力定义为在74℃条件下,30分钟内,以活性化的大马哈鱼精子dna作为模板/引物,催化10nmol脱氧核苷酸掺入反应成为酸不溶性物质所需的酶量。
储存于含有50mm tris hcl (ph8.1),0.1mm edta,1mm dtt,0.1% (v/v) nonidetp40, 0.1% (v/v) tween 20和50% (v/v)甘油的缓冲液,5units/μl。
-20℃
1. shown below is a pcr amplification of 1kb to 20kb fragmentsfrom λdna using dna polymerase.
figure 1. pcr amplification of 1-20kb fragments from λdna usingdna polymerase. 1u of enzyme was used for each50μl pcr. 5μl of pcr mixture was analyzed in each lane. lane1 showsa fragment of 1kb; lane2: 2kb; lane3: 3kb; lane4: 4kb; lane5: 5kb;lane6: 6kb; lane7: 8kb; lane8: 10kb; lane9: 12kb; lane10: 20kb.lanem shows genscript"s dna kb ladder (genscript, m101r).
2. shown below is a pcr amplification of 17.6kb fragments fromhuman genomic dna and 20kb fragments from λdna usingdna polymerase.
figure 2. pcr amplification of 17.6kb fragments (lanes2, 3, and 4)from human genomic dna and 20kb fragments (lanes6, 7, and 8) fromλdna using dna polymerase. all pcrs were performedin 50μl, and 3μl of reaction mixture was loaded in each lane.
lane1: 5udna polymerase was used to amplify17.6kb fragments from human genomic dna.
lanes2, 3 and 4: 1u, 2u, and 5u of dna polymerasewere used to amplify 17.6kb fragments from human genomic dna.
lane5: 5u kod dna polymerase was used to amplify 20kb fragmentsfrom λdna.
lanes6, 7 and 8: 1u, 2u and 5u of dna polymerasewere used to amplify 20kb fragment from λdna.
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