Poly(A) Polymerase, Yeast | E017

abm | Poly(A) Polymerase, Yeast | E017

Poly(A) Polymerase, Yeast catalyses the template independent addition of adenosine residues onto the 3' ends of polyribonucleotides. The use of ATP as a substrate leads to poly(A) tailing whereas substitution of cordycepin-5'-triphosphate (3'-dATP) for ATP results in addition of a single dA residue to the 3’-termini of the RNA. Neither ADP nor dATP can be used as substrates for this enzyme. Poly(A) Polymerase from yeast has been shown to be more effective at oligonucleotide-labeling and poly(A) tailing of long RNA templates than Poly(A) Polymerase from E. coli.

Concentration:

1 U/μl

Form:

N/A

Alternate Name:

N/A

Reaction Buffer:

N/A

Reaction:

N/A

Notes:

N/A

Application:

Restriction enzyme digestion of double-stranded DNA

Components:

EcoRI enzyme supplied with 10X Universal Restriction Enzyme Reaction Buffer

Inactivation:

65°C for 20 min

Source:

An E. coli strain that carries the modified EcoRI gene from E. coli RY13. The EcoRI enzyme recognizes and cuts the sequence G^AATTC.

Shipping conditions:

Dry ice

Storage conditions:

Store all components at -20°C.

Storag Buffer:

20 mM Tris-HCl (pH 8.0), 100 mM NaCl, 0.1 mM EDTA, 1 mM DTT, 0.1% Triton® X-100 and 50% (v/v) Glycerol.