Search
Citations & References (12)
Invitrogen™
Random Primers DNA Labeling System
The Random Primers DNA Labeling System is ideal for radioactively labeling DNA, particularly fragments under 1 kb. The Random PrimersRead more
| Catalog Number | Quantity |
|---|---|
| 18187013 | 30 Reactions |
Catalog number 18187013
Price (CNY)
6,415.00
Each
Quantity:
30 Reactions
Price (CNY)
6,415.00
Each
The Random Primers DNA Labeling System is ideal for radioactively labeling DNA, particularly fragments under 1 kb. The Random Primers DNA Labeling System:
––Yields >109 cpm/μg control DNA using [ α-32 P]-dCTP
–25 ng of DNA in one reaction
Performance and Quality Testing: Incorporation of a radioactively labeled nucleotide is verified using control DNA in a random primers labeling reaction.
––Yields >109 cpm/μg control DNA using [ α-32 P]-dCTP
–25 ng of DNA in one reaction
Performance and Quality Testing: Incorporation of a radioactively labeled nucleotide is verified using control DNA in a random primers labeling reaction.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Detection MethodRadioactive
Final Product TypeProbes (Labeled DNA)
Includes Label or DyeNo
Labeling MethodDirect Labeling
Labeling TargetDNA (General)
Label or Dye32P (Phosphorous-32)
Product TypeDNA Labeling System
Quantity30 Reactions
Shipping ConditionApproved for shipment on Wet or Dry Ice
Unit SizeEach
Contents & Storage
Components of the Random Primers DNA Labeling System are listed in the table to the right. Store at -20°C.
Frequently asked questions (FAQs)
How can I label COT-1 DNA?
Citations & References (12)
Citations & References
Abstract
Human biliverdin reductase is a leucine zipper-like DNA-binding protein and functions in transcriptional activation of heme oxygenase-1 by oxidative stress.
Journal:J Biol Chem
PubMed ID:11773068
Human biliverdin reductase (hBVR) is a serine/threonine kinase that catalyzes reduction of the heme oxygenase (HO) activity product, biliverdin, to bilirubin. A domain of biliverdin reductase (BVR) has primary structural features that resemble leucine zipper proteins. A heptad repeat of five leucines (L(1)--L(5)), a basic domain, and a conserved alanine
Activation of the androgen receptor N-terminal domain by interleukin-6 via MAPK and STAT3 signal transduction pathways.
Journal:J Biol Chem
PubMed ID:11751884
'The androgen receptor (AR) is a ligand-activated transcription factor that mediates the biological responses of androgens. However, non-androgenic pathways have also been shown to activate the AR. The mechanism of cross-talk between the interleukin-6 (IL-6) and AR signal transduction pathways was investigated in LNCaP human prostate cancer cells. IL-6 induced
PPARgamma knockdown by engineered transcription factors: exogenous PPARgamma2 but not PPARgamma1 reactivates adipogenesis.
Journal:Genes Dev
PubMed ID:11782439
'To determine functional differences between the two splice variants of PPARgamma (gamma1 and gamma2), we sought to selectively repress gamma2 expression by targeting engineered zinc finger repressor proteins (ZFPs) to the gamma2-specific promoter, P2. In 3T3-L1 cells, expression of ZFP55 resulted in >50% reduction in gamma2 expression but had no
Interaction of the Poliovirus Receptor CD155 with the Dynein Light Chain Tctex-1 and Its Implication for Poliovirus Pathogenesis.
Journal:J Biol Chem
PubMed ID:11751937
'The cellular receptor for poliovirus CD155 (or PVR) is the founding member of a new class of membrane-associated immunoglobulin-like proteins, which include the mouse tumor-associated antigen E4 (Tage4) and three proteins termed '
A trypanosome mitochondrial RNA polymerase is required for transcription and replication.
Journal:J Biol Chem
PubMed ID:11859084
'Understanding mitochondrial transcription is a requisite first step toward understanding the regulation of mitochondrial gene expression in kinetoplastids. Here we report the identification and functional characterization of a mitochondrial RNA polymerase (mtRNAP) from Trypanosoma brucei, the first trans-acting factor involved in kinetoplast mitochondrial transcription to be identified. Using sequences conserved