Propidium monoazide

Catalog No.: A43674
DNA-binding Dye
Propidium monoazide (PMA) is a cell-impermeant photoreactive DNA-binding dye that selectively targets double-stranded DNA (dsDNA). It effectively prevents the amplification of DNA derived from dead bacteria during polymerase chain reaction (PCR), enhancing both the specificity and sensitivity of PCR assays. Additionally, PMA serves as a click chemistry reagent, containing an azide group that participates in copper-catalyzed azide-alkyne cycloaddition (CuAAc) and strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with alkyne-containing molecules, DBCO, or BCN groups, facilitating advanced chemical labeling and analysis in research applications.
Grouped product items
Size Price Stock Qty
1mg
$320.00
In stock
Bulk Size
Bulk Discount
Free Delivery on orders over $500
Research use only. We do not sell to patients.

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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
Science VOLUME 369, ISSUE 6510 (2020)
Science VOLUME 356, ISSUE 6336 (2017)
Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
DescriptionPropidium monoazide (PMA) is a cell-impermeant photoreactive DNA-binding dye that selectively targets double-stranded DNA (dsDNA). It effectively prevents the amplification of DNA derived from dead bacteria during polymerase chain reaction (PCR), enhancing both the specificity and sensitivity of PCR assays. Additionally, PMA serves as a click chemistry reagent, containing an azide group that participates in copper-catalyzed azide-alkyne cycloaddition (CuAAc) and strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with alkyne-containing molecules, DBCO, or BCN groups, facilitating advanced chemical labeling and analysis in research applications.
Product Information
Catalog NumA43674
FormulaC27H32Cl2N6
Molecular Weight511.49
CAS Number91416-20-5
SMILES[N-]=[N+]=NC1=CC2=C(C3=C([N+](CCC[N+](CC)(CC)C)=C2C4=CC=CC=C4)C=C(N)C=C3)C=C1.[Cl-].[Cl-]
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