The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Nov. 08, 2022

Filed:

Jun. 08, 2021
Applicant:

New England Biolabs, Inc., Ipswich, MA (US);

Inventors:

Sriharsa Pradhan, Ipswich, MA (US);

Hang Gyeong Chin, Ipswich, MA (US);

George R. Feehery, West Newbury, MA (US);

Shuang-Yong Xu, Lexington, MA (US);

Vishnu Udayakumaran Nair Sunitha Kumary, Ipswich, MA (US);

Julie Beaulieu, Essex, MA (US);

Pierre O. Esteve, Ipswich, MA (US);

Assignee:

New England Biolabs, Inc., Ipswich, MA (US);

Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
C12Q 1/6869 (2018.01); C07K 14/31 (2006.01); C12N 9/22 (2006.01);
U.S. Cl.
CPC ...
C12Q 1/6869 (2013.01); C07K 14/31 (2013.01); C12N 9/22 (2013.01); C07K 2319/00 (2013.01);
Abstract

Compositions, methods and kits are provided for identifying the presence and location of a target in chromosomal DNA. A nicking endonuclease fused to a binding domain that binds to a constant region of an antibody (NEFP) is provided that may be used for binding to a target directly or via an antibody that binds to the target. The target may be a protein or structural feature of the DNA and its presence and location may correspond to a phenotype and/or pathology in a biopsy or other cell sample for diagnostic purposes. The background is reduced by the addition of a glycoaminoglycan (GAG) that reversibly inhibits binding of the NEFP to DNA. Nick translation in the presence of a strand displacing polymerase enables the incorporation of tagged nucleotides that (i) blocks re-nicking; (ii) facilitates immobilization of DNA fragments around the target for sequencing; and/or (iii) enables dye labelling of the chromosomal DNA within the cell nuclei for analysis by microscopy.


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