IFNGR2 (NM_005534) Human 3' UTR Clone

Specifications

Product Data
Product Name	IFNGR2 (NM_005534) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	AF-1; IFGR2; IFNGT1; IMD28
ACCN	NM_005534
Insert Size	584 bp
Sequence Data	Insert Sequence (showhide) >SC207624 3’UTR clone of NM_005534 The sequence shown below is from the reference sequence of NM_005534. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GAGCAAGAAGATGTTCTCCAAACGCTTTGAACCAAAGCATGGGCCTAGCCCACTGGCTCCCTGGAAGAG ATCAAGCCATCGGAGCTGCTAGAGTTCTGTCTGGACTTTCCAGAGACCAGTATTCCCTTTTGCTGCCTC TAAAAGGCCTGTCCCTGCAGACATGAGAGACAGCAGGTCTCATGGGGGTGACAAGCTTTTTTTTTTTTT CTTAAAGAATTTTCAAAATCAAATTCCAGAATGATTTTACGGAGATATCCCAGGAAAATTAAGGCTTCT CTTAAACACTAAAAAGGCATGTAATTGCTTGTTAGCAAAATGGATATGACACATCTCTGATACTTTTTT CATTATTGGTTGGGCTGAGCAGTCAGAAGACCTGGTCGTCGTCTTGACTTTGGCAAATGAGCCGGAGCC CCTTGGGCAGGTCACACAACCTGTCCCAGCGAGGGACACCGAGTGGCCCTTCATGTACATCCATGGTGT GCTGGCTTAAAATGTAATTAATCTTGTAAATATACTCCTAGTAATTTAAGATTTTGTTTTTAAACTGGA AATAAAAGATTGTATAGTGCATGTTTTTTAAA 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_005534.4
Synonyms	AF-1; IFGR2; IFNGT1; IMD28
Summary	This gene (IFNGR2) encodes the non-ligand-binding beta chain of the gamma interferon receptor. Human interferon-gamma receptor is a heterodimer of IFNGR1 and IFNGR2. Defects in IFNGR2 are a cause of mendelian susceptibility to mycobacterial disease (MSMD), also known as familial disseminated atypical mycobacterial infection. MSMD is a genetically heterogeneous disease with autosomal recessive, autosomal dominant or X-linked inheritance. [provided by RefSeq, Jul 2008]
Locus ID	3460
MW	22.5

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