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Research use only. Information, descriptions,
and specifications in this publication are subject
to change without notice.
Agilent Technologies shall not be liable for errors
contained herein or for incidental or consequential
damages in connection with the furnishing,
performance or use of this material.
© Agilent Technologies, Inc. 2006
Printed in the U.S.A. August 31, 2006
5989-4321EN
The Agilent Probe Advantage
Unlike other companies, Agilent
provides optimized and validated probe
design that delivers the high signal-tonoise ratios that are essential for the
success of ChIP-on-chip experiments.
We carefully design our probes using
stringent criteria.*
• 60-mer oligonucleotide probes provide
robust hybridization, critical for the
sensitivity and specificity that
ChIP-on-chip demands.
• Average probe spacing parameters
have been specifically optimized for
the ChIP method as compared to other
microarray applications.
• Repeat regions are masked to
significantly reduce nonspecific noise.
*Probes are designed with criteria including
optimal Tm, unique sequence, and self-structure
prediction.
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Product number
Slides/set
Minimum order
Microarrays/slide
Design ID numbers
Microarray format
Probe length
Probes/Transcript
Probe coverage
Agilent internal quality control probes
Sequence source
Feature size
Starting sample input
DNA required for labeling
Type of labeling
DNA required for hybridization
Hybridization volume
Specifications
Mouse Promoter Set
G4490A
2
5 sets (10 slides)
1
014716, 014717
244K
60 bases
~25 probes
~17,000 of the best defined
mouse transcripts and cover
–5.5 KB upstream to +2.5 KB
downstream from the transcriptional
start sites
~5000
UCSC mm7/NCBI release 35
(August 2005)
65 µm
0.5 x 10
7
–1 x 108cells
2 µg
Random priming using Klenow
with Cyanine 3 and Cyanine 5 nucleotides
5 µg per channel
500 µL