US2012322684A1PendingUtilityA1
G-csf protein having a deletion of an amino acid sequence corresponding to exon 3 for use as a diagnostic cancer marker
Est. expirySep 28, 2021(expired)· nominal 20-yr term from priority
C07K 16/243C12N 15/11C12Q 1/6886C12Q 2600/156
58
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Claims
Abstract
Disclosed are a method, a composition, a microarray, an antibody and a kit for diagnosis and prognosis of cancer, based on detection of deletion of the exon 3 region of G-CSF gene or levels of a mutated G-CSF protein having a deletion of an amino acid sequence corresponding to the exon 3 region, wherein the deletion of the exon 3 region of the G-CSF gene is used as a cancer biomarker.
Claims
exact text as granted — not AI-modified1 . (canceled)
2 . A mutated G-CSF protein having a deletion of an amino acid sequence corresponding to an exon 3 region for use as a diagnostic cancer marker.
3 - 8 . (canceled)
9 . A mutated G-CSF protein having a deletion of an amino acid sequence corresponding to an exon 3 region.
10 - 14 . (canceled)
15 . A mutated G-CSF mRNA or cDNA fragment having a deletion of an exon 3 region for use as a diagnostic cancer marker.
16 . A primer for use in amplification of a G-CSF gene in a G-CSF nucleic acid sample obtained from mammalian tissues or cells.
17 . The primer as set forth in claim 16 , wherein said primer is selected from the group consisting of the following nucleotide sequence pairs:
sense:
(SEQ ID NO. 1)
5′-ACCCCCCTGGGCCCTGCC-3′
and
antisense:
(SEQ ID NO. 2)
5′-TCAGGGCTGGGCAAGGTG-3′;
sense:
(SEQ ID NO. 1)
5′-ACCCCCCTGGGCCCTGCC-3′
and
antisense:
(SEQ ID NO. 5)
5′-CAGCTGCAGGGCCTGGCT-3′;
sense:
(SEQ ID NO. 1)
5′-ACCCCCCTGGGCCCTGCC-3′
and
antisense:
(SEQ ID NO. 6)
5′-CGCTATGGAGTTGGCTCAAGC-3′;
sense:
(SEQ ID NO. 1)
5′-ACCCCCCTGGGCCCTGCC-3′
and
antisense:
(SEQ ID NO. 9)
5′-CAGCTTCTCCTGGAGCGC-3′;
sense:
(SEQ ID NO. 3)
5′-ATCCAGGGCGATGGCGCAGCG-3′
and
antisense:
(SEQ ID NO. 2)
5′-TCAGGGCTGGGCAAGGTG-3′;
sense:
(SEQ ID NO. 3)
5′-ATCCAGGGCGATGGCGCAGCG-3′
and
antisense:
(SEQ ID NO. 5)
5′-CAGCTGCAGGGCCTGGCT-3′;
sense:
(SEQ ID NO. 3)
5′-ATCCAGGGCGATGGCGCAGCG-3′
and
antisense:
(SEQ ID NO. 6)
5′-CGCTATGGAGTTGGCTCAAGC-3′;
sense:
(SEQ ID NO. 4)
5′-TGTGCCACCTACAAGCTGTGC-3′
and
antisense:
(SEQ ID NO. 2)
5′-TCAGGGCTGGGCAAGGTG-3′;
sense:
(SEQ ID NO. 4)
5′-TGTGCCACCTACAAGCTGTGC-3′
and
antisense:
(SEQ ID NO. 5)
5′-CAGCTGCAGGGCCTGGCT-3′;
and
sense:
(SEQ ID NO. 4)
5′-TGTGCCACCTACAAGCTGTGC-3′
and
antisense:
(SEQ ID NO. 6)
5′-CGCTATGGAGTTGGCTCAAGC-3′.
18 . A diagnostic method for cancer comprising the steps of: (a) obtaining a G-CSF nucleic acid sample from mammalian tissues or cells; (b) amplifying a G-CSF region from the nucleic acid sample obtained; (c) detecting a deletion of exon 3 of said G-CSF gene in the amplified sample.Join the waitlist — get patent alerts
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