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2013 Promega catalogue

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Life<br />

Science<br />

Catalog<br />

<strong>2013</strong><br />

Worldwide Contact List<br />

Cell Signaling<br />

Cell ID System<br />

Product Size Cat.# Price ($)<br />

Cell ID System<br />

50 reactions G9500 Pls. Enq.<br />

Available Separately Size Cat.# Price ($)<br />

Water, Amplification Grade<br />

6,250 μl DW0991 Pls. Enq.<br />

Internal Lane Standard 600 150 μl DG1071 362<br />

DW0991, DG1071 For Laboratory Use. G9500 For Research Use Only. Not for Use in Diagnostic<br />

Procedures.<br />

Description: The Cell ID System provides the reagents required for<br />

successful and simple identification and authentication of human cell lines and<br />

detection of intra-species cell line cross-contamination. The Cell ID System<br />

uses short tandem repeat (STR) analysis of specific loci in the human genome<br />

through co-amplification and three-color detection of ten loci (nine STR loci and<br />

Amelogenin for gender identification), including D21S11, TH01, TPOX, vWA,<br />

Amelogenin, CSF1PO, D16S539, D7S820, D13S317 and D5S818. All ten loci<br />

are amplified simultaneously in a single tube. The Cell ID System includes<br />

a hot-start Taq DNA polymerase system in an enzyme mix for convenient<br />

room-temperature reaction assembly. Alleles, along with the allelic ladder and<br />

an internal lane standard that assists in assigning sizes for each locus, are<br />

resolved by capillary electrophoresis (CE) in a single injection, and CE data are<br />

analyzed using allele-calling software to generate a genetic profile of the cell line.<br />

These loci collectively provide a genetic profile with a random match probability<br />

of 1 in 2.92 × 10 9 .<br />

The Cell ID System is designed specifically for use with the Applied Biosystems<br />

® 3130 and 3130xl Genetic Analyzers, ABI PRISM ® 3100 and 3100-Avant<br />

Genetic Analyzers and ABI PRISM ® 310 Genetic Analyzer.<br />

Dye matrix generation is required on initial setup and is performed using the<br />

PowerPlex ® Matrix Standards, 310 (Cat.# DG4640), or PowerPlex ® Matrix<br />

Standards, 3100/3130 (Cat.# DG4650).<br />

Features:<br />

• Improved “Gold Standard” STR Analysis: The Cell ID System<br />

includes all loci used in the original PowerPlex ® 1.2 System plus the<br />

D21S11 locus for improved power of discrimination.<br />

• Simplified Data Interpretation: The Cell ID System allows<br />

co-amplification of ten loci to accurately discriminate between human cell<br />

lines without using a full forensic profile and includes allelic ladders for all<br />

ten loci to simplify data interpretation.<br />

• Simplified Amplification Setup: Inclusion of a hot-start Taq DNA<br />

polymerase allows room-temperature reaction assembly.<br />

• Internal Lane Standard 600: This marker offers the greatest precision<br />

available for DNA typing. It is designed for use in each capillary injection to<br />

increase the precision of your analyses.<br />

• Automatic Assignment of Genotypes: To make genotyping easier and<br />

more accurate, panels and bins files are available for download and are<br />

required for use with GeneMapper ® ID software. Use of GeneMapper ® 4.0<br />

software requires custom bin generation, and procedures can be found on<br />

the Cell ID System Analysis Support Software page at: www.promega.<br />

com/resources/tools/cell-id-system-analysis-support-software/<br />

Storage Conditions: Store at –20°C. The Primer Pair Mix, Allelic Ladder and<br />

Internal Lane Standard are light-sensitive and should be stored protected from<br />

light.<br />

Protocol<br />

Cell ID System Technical Manual<br />

Fluorescein:<br />

JOE:<br />

TMR:<br />

A<br />

D5S818<br />

vWA<br />

TH01<br />

D21S11<br />

D13S317 D7S820 D16S539 CSF1PO<br />

TPOX<br />

Part#<br />

TM074<br />

CXR:<br />

Size (bp) 100 200 300 400<br />

A = Amelogenin<br />

Allele ranges for the Cell ID System. STR fragments amplified by<br />

the Cell ID System are labeled with different dyes and are separated<br />

by capillary electrophoresis based on size. A size standard is included in<br />

each sample to determine the size of the Cell ID-amplified fragments.<br />

Fluorescein-labeled loci are shown in dark gray, JOE-labeled loci are<br />

shown in gray and TMR-labeled loci are shown in white. The CXR-labeled<br />

Internal Lane Standard 600 fragments are represented by black bars.<br />

7426MA<br />

Section<br />

Contents<br />

Table of<br />

Contents<br />

338<br />

For complete and up-to-date product information visit: www.promega.com/catalog

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