AMPD3 (NM_000480) Human 3' UTR Clone
CAT#: SC216053
3' UTR clone of adenosine monophosphate deaminase (isoform E) (AMPD3) transcript variant 1 for miRNA target validation
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CNY 5795.00
货期*
3周
规格
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Specifications
Product Data | |
Product Name | AMPD3 (NM_000480) Human 3' UTR Clone |
Vector | pMirTarget |
ACCN | NM_000480 |
Insert Size | 1725 bp |
Sequence Data |
>SC216053 3’UTR clone of NM_000480
The sequence shown below is from the reference sequence of NM_000480. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TCAGAAGAGATCACCGCCTTGACCAACTAGGTCCAGCATTTGACATGCATTTTAACTTTTTGGTTCAAT TTCAAGTCTGCTGTGGCTAATAGTGGTCAAGATTCCGAACTAGGACTTTCCTCTGTGAAGAGGATGCCT CTGAAGAAATTTTAAACTGGTGATTTTGGTTGCACTGCTCACTTTAAGAGTTAACATGCTCACTTGTTA GTATTTCTGAGTAACAAGATGGTGACTTCTCCTTGGGGATCTGGGAGCTGAGCACTTGTCTATACTTGT TCCTAATTTTCCAAGTATTTCTCTTGAAACTGCCAGTGCCTGAACTGTTGGGGCCAGGATTTTCCCTGG TCAGATGCCAAGTAACATGTGGTTTTCTGCCATACTTTTCTCCATTGGCCCAGGTAGGCTAATTGGTAG TTGTTCATTTCAGCCTCTGGATGGCTGGCTGCCTTAAACACAATCAATTTCAAAGCTCCATTTCATAAA GGGGCTACTTTGAAGGAGTTAAGATGGAAGACTTCCTTCTTGACAAATTGTGTTTTTAGTGAATTTCTT AAACCGTTTTATTTAGCCCTCCTTCCCTCTTTCTAGTTGGAAGCCAAATGTACTCATGAAAACAGCCAC TCCTATTCTGAGTCTTGGTTTCTTCACCTAGAAAGTGAGGGTTTGGACTAGATGAGTGGCTTTCAGGGT GTTCTGTGAATCTCCTCATGAATACTTTAGGGTAGGGGAGGGAAGGGAGTGAGTGATGCTCAGGGGCTG TCAAAGTGACTGCGTTCATCAGTTTTACACTGGGGCTGCTACATAATATTTTCATTTGAACGAAGAACT TCAAAAAGCACAGGACTAGATGATCTCTGTTCCTTTTGGCTCTAATATGCTACAACTGTAGGCCAATTA TCACTTTACCAATTAAGAGTTAGGCCAGATAAGTGAAATTTAACTTAAGGGCACACAGCTAATAAGTAA TAGGCCTAAACTGGATTTCCTTATTCCAAATCCTGTCTTTTCCCCACTATTCCATTAGACCCCACAAAT GTTAGTTGTGTGTGTGTGTGTGTGTGTTTTTAATCACTGTAACCGGATGCATTTTTTTAAGGCAAAATT TCTCCCTTATCTACTATGATGACTTCAGAAGATACAATGGTCCCAGGGGCCAAGTAGAAAGCATTTTTA AAGATTAATCTGAATTAAGCTTTATCAGTGTACTCTTTATCTGTGTTACTAGTGCCTGGTATGTAGTAG GTGCTCAATAAATGCATATTGAATAACTAAGTGAATTTCTTTTGGCAACTTTTTAAGGACATGTGCTCT TAGTACTTAAGAGGCTGCTCAAGGACCTTCCTATCTATTTCTGTGGTCAAATTCAGACTACAGGAGGTC TTTTTGAATCATTATAGTTAGAAGAAGAATCCAGTTTCTGCCTGTGAACTTATTTGACTTTAGATTGTC TCATCTTGTGACTTTATAATGCCTGTCCCCTCCACTGGTCAATTCAGCATATGGAAGTATAAATGCAGT CTTTTTACTAGGCAGATATATATGCTATCTTACAGCTAATTATGAAATTGAATGAAAATCCATTGTTAT CTTAGGGATTAGTTTTGAAAAGCCCCCGTTTATATACATTTGCCCTAACATAGGAAGTATTGTGTAGTT TCTCATTGTCATTTTATCTGTATCAAGTATCTTTTTTTAAATTGTTAAATAAAGTCAGCTAGGACTGTG ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG |
Restriction Sites | SgfI-MluI |
OTI Disclaimer | Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs). |
Reference Data | |
RefSeq | NM_000480.3 |
Summary | This gene encodes a member of the AMP deaminase gene family. The encoded protein is a highly regulated enzyme that catalyzes the hydrolytic deamination of adenosine monophosphate to inosine monophosphate, a branch point in the adenylate catabolic pathway. This gene encodes the erythrocyte (E) isoforms, whereas other family members encode isoforms that predominate in muscle (M) and liver (L) cells. Mutations in this gene lead to the clinically asymptomatic, autosomal recessive condition erythrocyte AMP deaminase deficiency. Alternatively spliced transcript variants encoding different isoforms of this gene have been described. [provided by RefSeq, Jul 2008] |
Locus ID | 272 |
MW | 65.3 |
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