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INFORMATION FOR CONTRIBUTORS {1992) each paragraph, subheads, and list items. Indicate on the disc: computer brand name, whether the disc contains a text or word- Aims and Scope processing file {name of software), and the disc format. Five hardcopy versions should also be submitted for use by referees Genes & Development welcomes high-quality research papers and editors. of general interest and biological significance in molecular bi- 3. Form. The following order is preferred: Title page, Ab- ology, molecular , and related areas. Publication time stract, Introduction, Results, Discussion, Methods, Acknowl- from acceptance of manuscript is between two and three edgments, References, Tables, Figure legends. The Title page months. 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CSH5 YES, QUALITY IS YOUR FIRST CHOICE FOR RNase HI!

1 2 3 4 5 6 Purity: Single Band on PAGE

phosphorylase B Easy to Use: 1 - 2 units / !~1 bovine serum albumin

ovalbumin Convenient: 3 Package Size available carbonic anhydrase 50, 100 and 400 units soybean trypsin inhibitor

lysozyme

Lane 1. The protein standards for molecular weight markers 2. The total soluble proteins from E. coli clone 3. The proteins purified by the first ion exchange chromatography 4. The more purified proteins by the second ion exchange chroma, tography 5. The purified RNase H by the final purification of gel filtration No other protein appeared on PAGE 6. Same as Lane I

Ribonuclease H from E. coli is an endonuclease that specifically degrades the RNA strand of DNA-RNA hybrids. RNase H is a key enzyme in several procedures including:

- Amplification by self-sustained sequence replication (3SR) - cDNA synthesis and <:loning where it is used to remove mRNA during second strand cDNA synthesis - Removal of poly (A) tails of mRNAs after hybridization with poly dT

"FOR RESEARCH USE ONLY. NOT FOR DRUG OR OTHER USES"

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Reader Service No. 865