Nitrocellulose, also called cellulose nitrate, is a chemically modified cellulose in which some or all of the available hydroxyl groups are converted into nitrate esters. The relevant connection is : the nitrogen is attached through oxygen, rather than directly to the carbon backbone as in a nitro group.[ref]
A cellulose repeat has three substitutable hydroxyls. For original atom bookkeeping, write its unmodified internal repeat as . Each replacement of by removes one hydrogen and adds one nitrogen and two oxygens. With substitutions per repeat, the corresponding composition is
At this gives . A fractional describes an average over repeat units, not fractional atoms in an individual unit; finite-chain end groups are omitted. “Nitrocellulose” consequently need not denote one unique substitution pattern or chain length.
A scientifically useful application is the nitrocellulose Western blot membrane. In a classic experiment, an electric field moved separated proteins from a gel onto a nitrocellulose sheet, preserving a spatial pattern accessible to antibodies. Transfer was quantitative for the tested urea-gel ribosomal proteins but not for the tested SDS gels.[ref]
Thus a retained band can locate a protein without proving that all of that protein was transferred. The receiving material, its retention and the detection method are separate parts of the measurement.

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Nitrocellulose is a highly flammable compound made from cellulose that has been chemically modified by the addition of nitric acid or other nitrogen-containing compounds. It is a type of nitroether and is classified as a nitrate ester. When cellulose (the structural component of plant cell walls) undergoes nitration, it replaces some of the hydroxyl groups (-OH) in cellulose with nitro groups (-NO2), resulting in a material that can be used in a variety of applications.