US2009029361A1PendingUtilityA1
Growth differentiation factor-7
Est. expiryJul 9, 2013(expired)· nominal 20-yr term from priority
A61P 37/00A61P 35/00C07K 14/51C07K 14/475A61P 25/00A61K 38/00
63
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Claims
Abstract
The present invention provides methods of using polynucleotides that hybridize specifically with a polynucleotide encoding GDF-7 to identify GDF-7 in a sample.
Claims
exact text as granted — not AI-modified1 . A method for detecting a polynucleotide encoding Growth Differentiation Factor-7 (GDF-7) in a sample comprising:
a) contacting the sample with an oligonucleotide probe that hybridizes specifically with a polynucleotide encoding GDF-7, wherein the oligonucleotide probe comprises at least about a 15 nucleotide portion of a nucleic acid molecule encoding a mammalian GDF-7; and b) detecting specific hybridization of the oligonucleotide probe to a polynucleotide in the sample, thereby detecting a polynucleotide encoding GDF-7 in the sample.
2 . The method of claim 1 , wherein the sample is selected from the group consisting of a tissue sample and a cell sample.
3 . The method of claim 1 , wherein the sample comprises neural tissue cells.
4 . The method of claim 1 , wherein detecting specific binding is performed in vitro.
5 . The method of claim 4 , wherein the polynucleotide to be contacted with the oligonucleotide probe is immobilized on a filter.
6 . The method of claim 1 , wherein the sample is obtained from a mammal.
7 . The method of claim 6 , wherein the mammal is selected from the group consisting of a mouse, rat, and human.
8 . The method of claim 1 , wherein the polynucleotide encodes the GDF-7 polypeptide of SEQ ID NO: 6.
9 . The method of claim 1 , wherein the oligonucleotide probe comprises at least about a 15 nucleotide portion of SEQ ID NO: 5.
10 . The method of claim 1 , wherein the oligonucleotide probe comprises a sequence selected from the group of sequences set forth as SEQ ID NO: 1 and SEQ ID NO: 2.
11 . The method of claim 1 , wherein detecting specific hybridization of the oligonucleotide probe comprises autoradiographic visualization of the probe.
12 . The method of claim 1 , wherein the oligonucleotide probe comprises a primer of a polymerase chain reaction (PCR) primer pair, whereby detecting specific hybridization of the oligonucleotide probe comprises performing PCR for 40 cycles at 94° C. for 1 minute, 50° C. for 2 minutes, and 72° C. for 2 minutes.
13 . The method of claim 12 , wherein the PCR primer pair comprises SEQ ID NO: 1 and SEQ ID NO: 2.
14 . A method of detecting a polynucleotide encoding Growth Differentiation Factor-7 (GDF-7) in a sample comprising:
a) contacting the sample with an oligonucleotide probe that hybridizes specifically with a polynucleotide encoding GDF-7, wherein the oligonucleotide probe comprises at least about a 15 nucleotide portion of a nucleic acid molecule encoding a mammalian GDF-7, and wherein the oligonucleotide probe comprises a primer of a polymerase chain reaction (PCR) primer pair comprising a forward primer and a reverse primer; and b) detecting specific hybridization of the oligonucleotide probe to a polynucleotide in the sample by performing PCR for 40 cycles at 94° C. for 1 minute, 50° C. for 2 minutes, and 72° C. for 2 minutes, thereby detecting a polynucleotide encoding GDF-7 in the sample.
15 . The method of claim 14 , wherein the PCR primer pair comprises SEQ ID NO: 1 and SEQ ID NO: 2.
16 . The method of claim 14 , wherein the sample is obtained from a mammal.
17 . The method of claim 16 , wherein the mammal is selected from the group consisting of a mouse, rat, and human.
18 . A biologically active C-terminal peptide fragment of a polypeptide consisting of the amino acid sequence as set forth in SEQ ID NO:6.
19 . The peptide fragment of claim 18 , wherein the fragment consists of 146 amino acids with a molecular weight of 14,900.
20 . The peptide fragment of claim 18 , wherein the fragment is SEQ ID NO: 7.Join the waitlist — get patent alerts
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