Fetuin A (AHSG) (NM_001622) Human 3' UTR Clone
CAT#: SC205503
3' UTR clone of alpha-2-HS-glycoprotein (AHSG) for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | Fetuin A (AHSG) (NM_001622) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | A2HS; AHS; APMR1; FETUA; HSGA |
ACCN | NM_001622 |
Insert Size | 418 bp |
Sequence Data |
>SC205503 3’UTR clone of NM_001622
The sequence shown below is from the reference sequence of NM_001622. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CCGGGGAGGATCAGACACTTCAAGGTCTAGGCTAGACATGGCAGAGATGAGGAGGTTTGGCACAGAAAA CATAGCCACCATTTTGTCCAAGCCTGGGCATGGGTGGGGGGCCTTGTCTGCTGGCCACGCAAGTGTCAC ATGCGATCTACATTAATATCAAGTCTTGACTCCCTACTTCCCGTCATTCCTCACAGGACAGAAGCAGAG TGGGTGGTGGTTATGTTTGACAGAAGGCATTAGGTTGACAACTTGTCATGATTTTGACGGTAAGCCACC ATGATTGTGTTCTCTGCCTCTGGTTGACCTTACAAAAACCATTGGAACTGTGACTTTGAAAGGTGCTCT TGCTAAGCTTATATGTGCCTGTTAATGAAAGTGCCTGAAAGACCTTCCTTAATAAAGAAGGTTCTAAGC TGAA 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_001622.4 |
Synonyms | A2HS; AHS; APMR1; FETUA; HSGA |
Summary | The protein encoded by this gene is a negatively-charged serum glycoprotein that is synthesized by hepatocytes. The encoded protein consists of two polypeptide chains, which are both cleaved from a proprotein encoded from a single mRNA. It is involved in several processes, including endocytosis, brain development, and the formation of bone tissue. Defects in this gene are a cause of susceptibility to leanness. [provided by RefSeq, Aug 2017] |
Locus ID | 197 |
MW | 16.3 |
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