Photobiotin acetate

Catalog No.: A92096
Biochemical Assay Reagent
Photobiotin acetate is a biochemical assay reagent that serves as a powerful biological probe for the investigation of protein interactions and enzymatic reactions. This compound features a photosensitive group that enables photochemical cross-linking with target molecules, facilitating the labeling and detection of proteins and nucleic acids. Photobiotin acetate forms stable covalent bonds during this crosslinking process and demonstrates high biocompatibility and biological activity, making it suitable for applications in enzymatic research, proteomics, and western blotting. Additionally, it can participate in click chemistry reactions, including copper-catalyzed azide-alkyne cycloaddition (CuAAc) and strain-promoted alkyne-azide cycloaddition (SPAAC) with complementary alkyne or cyclooctyne groups.
Grouped product items
Size Price Stock Qty
1mg
$1,120.00
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)
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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
DescriptionPhotobiotin acetate is a biochemical assay reagent that serves as a powerful biological probe for the investigation of protein interactions and enzymatic reactions. This compound features a photosensitive group that enables photochemical cross-linking with target molecules, facilitating the labeling and detection of proteins and nucleic acids. Photobiotin acetate forms stable covalent bonds during this crosslinking process and demonstrates high biocompatibility and biological activity, making it suitable for applications in enzymatic research, proteomics, and western blotting. Additionally, it can participate in click chemistry reactions, including copper-catalyzed azide-alkyne cycloaddition (CuAAc) and strain-promoted alkyne-azide cycloaddition (SPAAC) with complementary alkyne or cyclooctyne groups.
Product Information
Catalog NumA92096
FormulaC25H39N9O6S
Molecular Weight593.70
CAS Number96087-38-6
SMILESCC(O)=O.[N-]=[N+]=NC(C=C1)=CC([N+]([O-])=O)=C1NCCCN(C)CCCNC(CCCC[C@H]2[C@]3([H])[C@](NC(N3)=O)([H])CS2)=O
Useful Calculator

This calculator helps you calculate mass of compound based on solution concentration, volume and molecular weight in a specific solution using the formula:

Mass (mg) = Concentration (mM) × Volume (mL) × Molecular Weight (g/mol)

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This equation is commonly abbreviated as: C1V1 = C2V2

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