Promega Corporation

CE-Marked In Vitro Diagnostic Medical Device—Y Chromosome AZF Analysis

The Y Chromosome AZF Analysis System complies with EU Directive 98/79/EC on in vitro diagnostic medical devices. The Y Chromosome AZF Analysis System provides a multiplex PCR-based method to analyze the integrity of the human Y chromosome AZF region. The Y Chromosome AZF Analysis System is to be used as part of a diagnostic workup to characterize male infertility. This information is potentially useful for patients considering in vitro fertilization because deletions in the AZF region of the Y chromosome are passed on to male offspring produced by in vitro fertilization, resulting in infertility.

The Y Chromosome AZ...

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Y Chromosome AZF Analysis System

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Y Chromosome AZF Analysis System

 Components

  • Blue/Orange 6X Loading Dye

    G190B1 x 1ml
  • 50bp DNA Step Ladder

    G452C1 x 90μg
  • GoTaq® DNA Polymerase

    M300C1 x 200u
  • Male Genomic DNA

    MD115A1 x 50μl
  • Multiplex A Master Mix

    MD154A1 x 500μl
  • Multiplex B Master Mix

    MD155A1 x 500μl
  • Multiplex C Master Mix

    MD156A1 x 500μl
  • Multiplex D Master Mix

    MD157A1 x 500μl
  • Multiplex E Master Mix

    MD158A1 x 500μl
  • Nuclease-Free Water

    P119F1 x 1 each
25 reactions
- MD1631 Please Enquire


Storage Conditions

Store all components at –20°C. Avoid multiple freeze-thaw cycles.

For product intended use please see Patents & Disclaimers tab.

Example of amplification of male genomic DNA.Figure 1. Example of amplification of male genomic DNA.

Amplification of male genomic DNA (Part# MD115A) (lanes 1, 3, 5, 7, 9), as well as a negative DNA control (lanes 2, 4, 6, 8, 10), for each of the five Multiplex Master Mixes of the Y Chromosome AZF Analysis System.

Use Restrictions

MD1631 For In Vitro Diagnostic Use. This product is only available in certain countries.

Patents - Disclaimers

MD1631 U.S. Pat. No. 6,242,235, Australian Pat. No. 761757, Canadian Pat. No. 2,335,153 and other patents and patents pending.

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