URP2 (FERMT3) (NM_178443) Human 3' UTR Clone

Specifications

Product Data
Product Name	URP2 (FERMT3) (NM_178443) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	KIND3; MIG-2; MIG2B; UNC112C; URP2; URP2SF
ACCN	NM_178443
Insert Size	429 bp
Sequence Data	Insert Sequence (showhide) >SC205607 3’UTR clone of NM_178443 The sequence shown below is from the reference sequence of NM_178443. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CAGCTCACCGGGGGCCATGAGGCCTTCTGAGGGCTGTCTGATTGCCCCTGCCCTGCTCACCACCCTGTC ACAGCCACTCCCAAGCCCACACCCACAGGGGCTCACTGCCCCACACCCGCTCCAGGCAGGCACCCAGCT GGGCATTTCACCTGCTGTCACTGACTTTGTGCAGGCCAAGGACCTGGCAGGGCCAGACGCTGTACCATC ACCCAGGCCAGGGATGGGGGTGGGGGTCCCTGAGCTCATGTGGTGCCCCCTTTCCTTGTCTGAGTGGCT GAGGCTGATACCCCTGACCTATCTGCAGTCCCCCAGCACACAAGGAAGACCAGATGTAGCTACAGGATG ATGAAACATGGTTTCAAACGAGTTCTTTCTTGTTACTTTTTAAAATTTCTTTTTTATAAATTAATATTT TATTGTTGGATCCTC 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_178443.3
Synonyms	KIND3; MIG-2; MIG2B; UNC112C; URP2; URP2SF
Summary	Kindlins are a small family of proteins that mediate protein-protein interactions involved in integrin activation and thereby have a role in cell adhesion, migration, differentiation, and proliferation. The protein encoded by this gene has a key role in the regulation of hemostasis and thrombosis. This protein may also help maintain the membrane skeleton of erythrocytes. Mutations in this gene cause the autosomal recessive leukocyte adhesion deficiency syndrome-III (LAD-III). Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jan 2010]
Locus ID	83706
MW	15.6

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