IKB alpha (NFKBIA) (NM_020529) Human 3' UTR Clone

Specifications

Product Data
Product Name	IKB alpha (NFKBIA) (NM_020529) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	EDAID2; IKBA; MAD-3; NFKBI
ACCN	NM_020529
Insert Size	530 bp
Sequence Data	Insert Sequence (showhide) >SC206945 3’UTR clone of NM_020529 The sequence shown below is from the reference sequence of NM_020529. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GTGTTTGGAGGCCAGCGTCTGACGTTATGAGCGCAAAGGGGCTGAAAGAACATGGACTTGTATATTTGT ACAAAAAAAAAGTTTTATTTTTCTAAAAAAAGAAAAAAGAAGAAAAAATTTAAAGGGTGTACTTATATC CACACTGCACACTGCCTGGCCCAAAACGTCTTATTGTGGTAGGATCAGCCCTCATTTTGTTGCTTTTGT GAACTTTTTGTAGGGGACGAGAAAGATCATTGAAATTCTGAGAAAACTTCTTTTAAACCTCACCTTTGT GGGGTTTTTGGAGAAGGTTATCAAAAATTTCATGGAAGGACCACATTTTATATTTATTGTGCTTCGAGT GACTGACCCCAGTGGTATCCTGTGACATGTAACAGCCAGGAGTGTTAAGCGTTCAGTGATGTGGGGTGA AAAGTTACTACCTGTCAAGGTTTGTGTTACCCTCCTGTAAATGGTGTACATAATGTATTGTTGGTAATT ATTTTGGTACTTTTATGATGTATATTTATTAAACAGATTTTTACAAA 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_020529.3
Synonyms	EDAID2; IKBA; MAD-3; NFKBI
Summary	This gene encodes a member of the NF-kappa-B inhibitor family, which contain multiple ankrin repeat domains. The encoded protein interacts with REL dimers to inhibit NF-kappa-B/REL complexes which are involved in inflammatory responses. The encoded protein moves between the cytoplasm and the nucleus via a nuclear localization signal and CRM1-mediated nuclear export. Mutations in this gene have been found in ectodermal dysplasia anhidrotic with T-cell immunodeficiency autosomal dominant disease. [provided by RefSeq, Aug 2011]
Locus ID	4792
MW	20.2

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