Assays for measuring nucleic acids
US-2024226890-A1 · Jul 11, 2024 · US
US9382579B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9382579-B2 |
| Application number | US-201414208728-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 13, 2014 |
| Priority date | Mar 2, 2012 |
| Publication date | Jul 5, 2016 |
| Grant date | Jul 5, 2016 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
An apparatus comprises an antenna pattern precursor, wherein the antenna pattern precursor includes a plurality of sensitive regions; and electromagnetically functionalized DNA/nanoparticle complex(es) that individualize the ability to transition between the precursor antenna electrical and resonant frequency characteristics, and activated antenna electrical and resonant frequency characteristics through DNA hybridization of the specific sequences contained in the electromagnetically functionalized DNA/nanoparticle complex(es).
Opening claim text (preview).
We claim: 1. An apparatus configured for a detection of DNA sequence(s), said apparatus comprising; (a) a radiating antenna unit precursor comprising: (i) a substrate, (ii) a plurality of disconnected conductive wire segments attached to and disposed substantially parallel to a surface of said substrate, (iii) a plurality of interconnects on said surface configured to interconnect at least two of said plurality of disconnected conductive wire segments, (iv) a plurality of gap regions, each spanning a distance between two conductive wire segments from said plurality of wire segments, (v) a plurality of different marker electromagnetically functionalized nanoparticle (EMFNP)/DNA sequences disposed within some of said gap regions, each marker EMFNP/DNA sequence comprising marker DNAs coupled to base EMFNPs, and (vi) said plurality of marker EMFNP/DNA sequences defining a radio frequency (RF) response from said conductive wire elements of said radiating antenna unit, said RF response determined by a geometry of said radiating antenna unit and a presence of different marker EMFNP/DNAC sequences bound to different regions between said conductive wire segments of said radiating antenna unit; (b) a separate RF analyzer unit disposed at a distance from said radiating antenna unit and configured to determine said RF response of said radiating antenna unit, said RF analyzer unit comprising: an RF transmitter, an RF receiver, and an RF signal analysis section; (i) said RF transmitter configured to transmit a plurality of frequencies toward said radiating antenna unit, (ii) said RF receiver configured to receive said RF response from said radiating antenna unit at said plurality of frequencies transmitted by said RF transmitter section toward said radiating antenna unit, (iii) said RF receiver configured to receive an RF response above 300 Mhz from said radiating antenna unit, (iv) said RF transmitter configured to transmit electromagnetic energy radiation towards said radiating antenna unit above 300 Mhz, (v) said RF transmitter configured to transmit electromagnetic energy radiation within a substantially continuous range of frequencies, (vi) said RF transmitter and said RF receiver configured to only transmit and receive electromagnetic energy radiation substantially at a same frequency simultaneously, and (vii) said RF signal analysis section configured to determine if a comparative response at a received frequency has been met; wherein a key solution containing complementary EMFNP/DNA sequences applied to said radiating antenna unit causes at least one EMFNP/DNA sequence within the key solution to hybridize with marker EMFNP/DNA sequence within said gap regions, and further causes change in electrical properties of said gap regions and a change in an overall RF response from said radiating antenna unit being received at said RF receiver; and wherein a key solution containing non-complementary EMFNP/DNA complexes applied to said radiating antenna unit will not hybridize with marker EMFNP/DNA sequences within said gap regions and will not change overall RF response from said radiating antenna unit.
Nucleic acid detection involving sensors · CPC title
Investigating or analysing materials by the use of microwaves or radio waves, i.e. electromagnetic waves with a wavelength of one millimetre or more (G01N3/00 - G01N17/00, G01N24/00 take precedence) · CPC title
Single/double strand conformational analysis, i.e. SSCP/DSCP · CPC title
being a sensor, e.g. electrode · CPC title
Nucleic acid dedicated to use as a hidden marker/bar code, e.g. inclusion of nucleic acids to mark art objects or animals · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.