US2015177240A1PendingUtilityA1
Nogo Receptor Binding Protein
Est. expiryMar 19, 2023(expired)· nominal 20-yr term from priority
A61P 9/10A61P 9/00A61P 43/00A61P 25/00A61P 25/14A61P 25/16A61P 25/02A61P 25/28A61P 21/02C07K 2319/30C07K 14/70571G01N 33/5058C07K 16/2803C12N 5/0619C07K 16/18A61K 38/00C12N 2500/46G01N 33/6896G01N 33/56966C07K 14/4702A61P 3/10C12N 15/11C12N 15/63A61K 38/17C12N 15/62
64
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Claims
Abstract
The invention provides Sp35 polypeptides and fusion proteins thereof, Sp35 antibodies and antigen-binding fragments thereof and nucleic acids encoding the same. The invention also provides compositions comprising, and methods for making and using, such Sp35 antibodies, antigen-binding fragments thereof, Sp35 polypeptides and fusion proteins thereof.
Claims
exact text as granted — not AI-modified1 - 57 . (canceled)
58 . A method for identifying an oligodendrocyte in a tissue sample, the method comprising contacting the tissue sample with an anti-Sp35 antibody or an Sp35-binding fragment thereof and an anti-O4 oligodendrocyte marker antibody or an O4-binding fragment thereof, wherein a cell that specifically binds both the anti-Sp35 antibody or Sp35-binding fragment thereof and the anti-O4 antibody or O4-binding fragment thereof is identified as an oligodendrocyte.
59 . The method of claim 58 , wherein the tissue sample is a spinal cord sample.
60 . The method of claim 58 , wherein the tissue sample is a primary granular neuron culture.
61 . The method of claim 58 , wherein the tissue sample is a frontal cortex sample.
62 . The method of claim 58 , wherein the tissue sample is a posterior cortex sample.
63 . The method of claim 58 , wherein the tissue sample is an entorhinal cortex sample.
64 . The method of claim 58 , wherein the tissue sample is a hippocampus sample.
65 . The method of claim 58 , wherein the tissue sample is an olfactory bulb sample.
66 . The method of claim 58 , wherein the tissue sample is selected from the group consisting of a striatum sample, a thalamus sample, a cerebellum sample, a midbrain sample, a pons sample, and a medulla sample.
67 . A method for identifying a neuron in a tissue sample, the method comprising contacting the tissue sample with an anti-Sp35 antibody or an Sp35-binding fragment thereof and an anti-βIII tubulin neuronal marker antibody or an βIII tubulin-binding fragment thereof, wherein a cell that specifically binds both the anti-Sp35 antibody or Sp35-binding fragment thereof and the anti-βIII tubulin antibody or βIII tubulin-binding fragment thereof is identified a neuron.
68 . The method of claim 67 , wherein the tissue sample is a spinal cord sample.
69 . The method of claim 67 , wherein the tissue sample is a primary granular neuron culture.
70 . The method of claim 67 , wherein the tissue sample is a frontal cortex sample.
71 . The method of claim 67 , wherein the tissue sample is a posterior cortex sample.
72 . The method of claim 67 , wherein the tissue sample is an entorhinal cortex sample.
73 . The method of claim 67 , wherein the tissue sample is a hippocampus sample.
74 . The method of claim 67 , wherein the tissue sample is an olfactory bulb sample.
75 . The method of claim 67 , wherein the tissue sample is selected from the group consisting of a striatum sample, a thalamus sample, a cerebellum sample, a midbrain sample, a pons sample, and a medulla sample.
76 . A method for inhibiting the homotypic interaction of Sp35 or modulating Sp35 interaction with NgR1, the method comprising contacting Sp35 with an oligopeptide of any one of SEQ ID NOs. 10-13.
77 . The method of claim 76 , wherein the method is for inhibiting the homotypic interaction of Sp35.Join the waitlist — get patent alerts
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