IL2 Receptor gamma (IL2RG) (NM_000206) Human 3' UTR Clone
CAT#: SC204808
3' UTR clone of interleukin 2 receptor gamma (severe combined immunodeficiency) (IL2RG) for miRNA target validation
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CN¥ 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 | IL2 Receptor gamma (IL2RG) (NM_000206) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | CD132; CIDX; IL-2RG; IMD4; P64; SCIDX; SCIDX1 |
ACCN | NM_000206 |
Insert Size | 362 bp |
Sequence Data |
>SC204808 3’UTR clone of NM_000206
The sequence shown below is from the reference sequence of NM_000206. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CCATGTTACACCCTAAAGCCTGAAACCTGAACCCCAATCCTCTGACAGAAGAACCCCAGGGTCCTGTAG CCCTAAGTGGTACTAACTTTCCTTCATTCAACCCACCTGCGTCTCATACTCACCTCACCCCACTGTGGC TGATTTGGAATTTTGTGCCCCCATGTAAGCACCCCTTCATTTGGCATTCCCCACTTGAGAATTACCCTT TTGCCCCGAACATGTTTTTCTTCTCCCTCAGTCTGGCCCTTCCTTTTCGCAGGATTCTTCCTCCCTCCC TCTTTCCCTCCCTTCCTCTTTCCATCTACCCTCCGATTGTTCCTGAACCGATGAGAAATAAAGTTTCTG TTGATAATCATCAAAAA 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_000206.3 |
Synonyms | CD132; CIDX; IL-2RG; IMD4; P64; SCIDX; SCIDX1 |
Summary | The protein encoded by this gene is an important signaling component of many interleukin receptors, including those of interleukin -2, -4, -7 and -21, and is thus referred to as the common gamma chain. Mutations in this gene cause X-linked severe combined immunodeficiency (XSCID), as well as X-linked combined immunodeficiency (XCID), a less severe immunodeficiency disorder. [provided by RefSeq, Mar 2010] |
Locus ID | 3561 |
MW | 13.7 |
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