Suspension Reagent to remove Hemoglobin interference for PCR
- Suitable for infectious disease research or rigorous analysis for whole blood or heavily hemolyzed samples
- Scaleable suspension reagent
- Robust and simple, no phenol/chloroform or ammonium sulfate precipitation
- High Yield – free and soluble DNA or RNA is highly recoverable
- > 95% Hemoglobin and Protein removal from whole blood lysates & dried blood cards
- Eliminates inhibitory effects of heme for PCR applications
- Compatible with silica-type final isolation preps
Some infectious viruses are known or suspected to be associated with red cells, such as Zika and West Nile viruses. So to detect their presence, it is becoming increasingly apparent to use whole blood, rather than plasma alone, as a starting sample type. However, the presence of hemoglobin from whole blood lysates is challenging for PCR because of the large amount of hemoglobin present. HemogloBind™ Nucleic Acid is designed to efficiently remove hemoglobin while maintaining very high recovery of nucleic acids, both RNA and DNA.
MATERIALS
Materials required | 5 ml | 50 ml |
HemogloBind™ Nucleic Acid suppliedas Suspension Reagent in 10 % Isopropanol | 5ml (25 prep) | 50ml (200 prep) |
Microfuge Spin-X type Filters | 25supplied | Recommended (Notsupplied) |
3M Guanidine ThioCyanate (orequivalent) | Notsupplied | Notsupplied |
Wide bore pipette tips | Suggested(Not Supplied) |
HemogloBind™ Nucleic Acid 5ml (includes Spin filters) | H0250-05 |
HemogloBind™ Nucleic Acid 50ml (reagent only) | H0250-50 |
Click Here To View HemogloBind™ Product Sheet
美国BSG(BiotechSupportGroup""LLC)公司是一家公司是一家全球知名的蛋白质组和基因组样本预处理的公司,是这个领域公认的领导者,该公司将其发明的专利表面化学技术应用生物学领域,比其他方法如亲合技术,苯酚法有绝对的优势。由于技术上的领先,使得BSG公司的产品广泛被美国国家基因组研究所,斯坦福大学等重要机构使用。
美国BSG(Biotech Support Group,LLC)公司是一家公司是一家全球知名的蛋白质组和基因组样本预处理的公司,是这个领域公认的*,该公司将其发明的表面化学技术应用生物学领域,比其他方法如亲合技术,苯酚法有绝对的优势。由于技术上的,使得BSG公司的产品广泛被美国国家基因组研究所,斯坦福大学等重要机构使用。(http://www.biotechsupportgroup。。com/) 目前我司成功取得美国BSG中国总代理,BSG各大产品均可在我司查询订购。 分子生物学 Ambion,Biosearch Technologies,Biotium,BPS bioscience,Dharmacon,Glen Research,HYQ ,Lucigen, lumiprobe,MO BIO,Molecular probes,NEB,Qiagen 细胞生物学 AddEXBIO,Cellgro,Echelon,Equitech,Gemini,Gibco,InvivoGen,Mlltenyi,Partec,Spherotech,Stemcell Abbiotec,Abcam,ABD SEROtec,Abnova,ADI,Antibodies-Online,AssayPro,Biorbyt,BioVision,BTI,Cellgro,CST,chromotek,Covance,Echelon,Endocrine Tech,Epitomics ,FD Neuro Technologies,Fitzgerald,GeneTex,GenWay,Gibco,Invitrogen,Invivogen,Jackson,Lifespan,LKT Labs,Miltenyi,Novex,Novus,Phoenix peptide,Pierece,,Plantmedia,Prospec,R&D,Spherotech,Stemcell,Trevigen,Santa cruz,,Separopore,USBIo,Vector Beckman coulter,BD,Biolegend,Affymetrix eBioscience,Tonbo A.G.Scientific,American Peptide,Apollo scientific,Cargille Lbs,Cayman,Nanocs,polysciences,Sigma,Tocris 诊断 Biocare,Biospacific,DIARECT,Fujirebio Diagnostics,Roche,Kamiya Epicentre,Ion Torrent,KAPA Biosystems 仪器/耗材 Applied Biosystems,Agilent,BD,Beckman coulter,Bio-Rad,GE,Perkin Elmer,Millipore,Parafilm,Uniequip
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请教各位老师,
文献中检测细胞的活性有的用“NADPHdehydrogenase(NADPH脱氢酶)”有的用“NADPHdiaphorase(NADPH黄递酶)”
它们是同一种酶吗?它们的功能是什么?检测它们的活性是否能够评估细胞的活性。
不胜感激
如果能分解,那小肠液中的消化酶如何大量共存,如果不能
那它如何识别其他蛋白质物质是不是消化酶?
反应体系如下:
plasmid10ul
10xKbuffer5ul
KpnI1ul
BamHI1ul注意千万不可多加总酶量必须<4%
ddH20upto50ul
总体积改变加酶量按比例改变.
明白了么,少年?
有谁用碧云天的过氧化氢酶检测试剂盒,在试剂盒的准备工作中,过氧化氢的实际浓度=22.94*A240,我测出来的吸光度是3.3左右,那么乘以22.94就等于76多点,再乘以之前的稀释倍数,大约就是7600mM左右,这样跟说明书中说道的1M相差太多,感觉不对啊,稀释的肯定是没有错的,但是不知道哪里出了错,怀疑说明书就有问题呢,有人做过这个实验吗?能不能准确测出过氧化氢浓度吗?有测过的人帮忙指点一下啊,不知道应该怎么做