DIG-High Prime DNA Labeling and Detection Starter Kit I
For 12 random-primed DNA labeling reactions with DIG-11-dUTP, alkali-labile, and 24 color detection reactions with NBT/BCIP.
For life science research only. Not for use in diagnostic procedures.
Product No. :11745832910
Pack Size：
1 kit for up to 12 labeling reactions and detection of 24 blots, 10 ng to 3 μg DNA per assay, blots of 100 cm2
Overview：
Convenient kit for random-primed labeling of DNA templates with DIG-11-dUTP, alkali-labile, and color detection of the DIG-labeled hybrids. In this method, the complementary DNA strand of denatured DNA is synthesized by Klenow polymerase using the 3'-OH termini of the random oligonucleotides as primers.This kit was assembled with convenience in mind, offering a ready-made blocking solution, combined stock solution of NBT/BCIP, and DIG Easy Hyb granules. The DIG-High Prime mixture includes stabilized Klenow Enzyme, nucleotides, primers, and reaction buffer, all in one convenient reagent.
Contents
DIG-High Prime, 5x concentrated
DIG-labeled Control DNA (5 μg/ml), pBR328 (linearized with BamH I)
DNA Dilution Buffer
Anti-digoxigenin-AP Conjugate
NBT/BCIP Stock Solution, concentrated
Blocking Solution, 10x concentrated
DIG Easy Hyb Granules
Application：
DIG-High Prime is used for the highly efficient random-primed labeling of DNA probes with DIG-11-dUTP, alkali-labile. DIG-labeled probes are generated at high yield within one hour or after overnight incubation. DIG-High Prime-labeled DNA probes are used in a variety of hybridization techniques:
Southern blots
Northern blots
Dot blots
Colony and plaque hybridizations
For all types of filter hybridization
For single-copy gene detection in total genomic DNA, even from organisms with high complexity, for example, human, barley, and wheat
Sample Materials
Principle
The DIG High Prime DNA Labeling and Detection Starter Kit I uses digoxigenin (DIG), a steroid hapten, to label DNA probes for hybridization and subsequent color detection by enzyme immunoassay. The "random primed" DNA labeling method originally developed by Feinberg and Vogelstein is based on the hybridization of oligonucleotides of all possible sequences to the denatured DNA to be labeled. The input DNA serves as a template for the synthesis of labeled DNA, and is not degraded during the reaction, making it possible to label minimal amounts of DNA (10 ng) with this method. The complementary DNA strand is synthesized by Klenow polymerase using the 3'-OH termini of the random oligonucleotides as primers. Modified deoxyribonucleoside triphosphates, labeled with digoxigenin present in the reaction are incorporated into the newly synthesized complementary DNA strand.
Quality
Function tested in a dot blot.