alpha 1 Antichymotrypsin (SERPINA3) (NM_001085) Human 3' UTR Clone
CAT#: SC203563
3' UTR clone of serpin peptidase inhibitor clade A (alpha-1 antiproteinase antitrypsin) member 3 (SERPINA3) for miRNA target validation
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CNY 4845.00
货期*
3周
规格
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Specifications
Product Data | |
Product Name | alpha 1 Antichymotrypsin (SERPINA3) (NM_001085) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | AACT; ACT; GIG24; GIG25 |
ACCN | NM_001085 |
Insert Size | 269 bp |
Sequence Data |
>SC203563 3’UTR clone of NM_001085
The sequence shown below is from the reference sequence of NM_001085. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AGCAAAGTCACCAATCCCAAGCAAGCCTAGAGCTTGCCATCAAGCAGTGGGGCTCTCAGTAAGGAACTT GGAATGCAAGCTGGATGCCTGGGTCTCTGGGCACAGCCTGGCCCCTGTGCACCGAGTGGCCATGGCATG TGTGGCCCTGTCTGCTTATCCTTGGAAGGTGACAGCGATTCCCTGTGTAGCTCTCACATGCACAGGGGC CCATGGACTCTTCAGTCTGGAGGGTCCTGGGCCTCCTGACAGCAATAAATAATTTCGTTGGA 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_001085.5 |
Synonyms | AACT; ACT; GIG24; GIG25 |
Summary | The protein encoded by this gene is a member of the serpin family of proteins, a group of proteins that inhibit serine proteases. This gene is one in a cluster of serpin genes located on the q arm of chromosome 14. Polymorphisms in this protein appear to be tissue specific and influence protease targeting. Variations in this protein's sequence have been implicated in Alzheimer's disease, and deficiency of this protein has been associated with liver disease. Mutations have been identified in patients with Parkinson disease and chronic obstructive pulmonary disease. [provided by RefSeq, Jun 2020] |
Locus ID | 12 |
MW | 9.1 |
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