Arginase 1 (ARG1) (NM_000045) Human 3' UTR Clone
CAT#: SC205656
3' UTR clone of arginase liver (ARG1) for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
Cited in 1 publication. |
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经常一起买 (2)
Specifications
Product Data | |
Product Name | Arginase 1 (ARG1) (NM_000045) Human 3' UTR Clone |
Vector | pMirTarget |
ACCN | NM_000045 |
Insert Size | 451 bp |
Sequence Data |
>SC205656 3’UTR clone of NM_000045
The sequence shown below is from the reference sequence of NM_000045. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CCTATTGACTACCTTAACCCACCTAAGTAAATGTGGAAACATCCGATATAAATCTCATAGTTAATGGCA TAATTAGAAAGCTAATCATTTTCTTAAGCATAGAGTTATCCTTCTAAAGACTTGTTCTTTCAGAAAAAT GTTTTTCCAATTAGTATAAACTCTACAAATTCCCTCTTGGTGTAAAATTCAAGATGTGGAAATTCTAAC TTTTTTGAAATTTAAAAGCTTATATTTTCTAACTTGGCAAAAGACTTATCCTTAGAAAGAGAAGTGTAC ATTGATTTCCAATTAAAAATTTGCTGGCATTAAAAATAAGCACACTTACATAAGCCCCCATACATAGAG TGGGACTCTTGGAATCAGGAGACAAAGCTACCACATGTGGAAAGGTACTATGTGTCCATGTCATTCAAA AAATGTGATTTTTTATAATAAACTCTTTATAACAAGA 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_000045.4 |
Summary | Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type I isoform encoded by this gene, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011] |
Locus ID | 383 |
MW | 17.8 |
Citations (1)
The use of this cDNA Clones has been cited in the following citations: |
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The Role of Arginine Metabolism in Oral Tongue Squamous Cell Carcinoma
,null,
Cancers
,PubMed ID 34885177
[ARG1]
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