Test
Designed to amplify cDNA only from full-length, capped mRNA, usually producing a single band after PCR
Format | Kit |
---|---|
Reverse Transcriptase | M-MLV |
Final Product Type | cDNA |
Product Type | RLM-RACE Kit |
Quantity | 1 Kit |
Optimal Reaction Temperature | 42°C |
For Use With (Application) | cDNA Libraries & Library Construction |
Product Line | Ambion™, FirstChoice™ |
Uses T7 capsid protein to display peptides or proteins on surface of phage.
Illumina-compatible next-gen sequencing (NGS) libraries from as little as 50ng of starting DNA. DNA fragmentation and transposon-tagging are accomplished in one step.
Offers efficient and convenient method for size-fractioning double-stranded cDNA (1)
Converts up to 1μg of total RNA preparation or 100ng of control RNA into cDNA in one reaction
Displays peptides up to about 50 amino acids in size.
Uses T7 capsid protein to display peptides or proteins on surface of phage.
CloneMiner™ II cDNA Library Construction Kit
Suitable for rapid amplification of cDNA ends (RACE) between defined point in mRNA and the 5' end
These untagged vectors are used for inducible expression of proteins in E. coli and cell-free systems using the T7 RNA polymerase promoter. Supplied as vectors used with the Flexi Cloning System.
HaloTag™ Cloning Starter Kit: designed to use Flexi Cloning System to clone protein coding sequences into mammalian HaloTag™ expression vectors; clone and transfer gene sequences into C- or N-terminus of HaloTag™ Flexi CMV Deletion Vectors.
The Flexi Vector System is a simple, yet powerful, directional cloning method for protein-coding sequences.
These vectors are used for inducible expression of N-terminal GST-tagged fusion proteins in E. coli and cell-free systems using the T7 RNA polymerase promoter.
The Flexi Vector System is a simple, yet powerful, directional cloning method for protein-coding sequences.
Designed for high-level expression of proteins in mammalian cells from the CMV promoter without a selectable marker