Laminin (LAMA1) (NM_005559) Human 3' UTR Clone
CAT#: SC202358
3' UTR clone of laminin alpha 1 (LAMA1) for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
Product images
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经常一起买 (2)
Specifications
Product Data | |
Product Name | Laminin (LAMA1) (NM_005559) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | LAMA; PTBHS; S-LAM-alpha |
ACCN | NM_005559 |
Insert Size | 367 bp |
Sequence Data |
>SC202358 3’UTR clone of NM_005559
The sequence shown below is from the reference sequence of NM_005559. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CTTCATTCCTGTCCTGGGACCGAGTCCTGAACTTCAAGCAGAATCCTCAGTTGGAATCATTGCTAATAT TTTGAGGAGAAGTGTATGTGTGAATTAAGAATCTCTTCAGTTCATATTTCATTTCCAACTCAGGTTAAG TGTTTCTGGGGAGAGATGTTGTGTTTACGTTACACTAAAACCACATGTGCAACAAATACCTCCATTAAA TGGTCTAAAATGTAAATTGAATTCCCTGGCTCTCTTTTTAAACGTATTTTTAAAAAAATCTTTATACAC ATTGAATGTTCTGTTGATTACTTGATAGTATTTTATGTTTTTCATTTTGAGCTTTTTAAAAAAGTATCA ATACAGATGATAACAGATCAGA 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_005559.4 |
Synonyms | LAMA; PTBHS; S-LAM-alpha |
Summary | This gene encodes one of the alpha 1 subunits of laminin. The laminins are a family of extracellular matrix glycoproteins that have a heterotrimeric structure consisting of an alpha, beta and gamma chain. These proteins make up a major component of the basement membrane and have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, neurite outgrowth and metastasis. Mutations in this gene may be associated with Poretti-Boltshauser syndrome. [provided by RefSeq, Sep 2014] |
Locus ID | 284217 |
MW | 14.5 |
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