ROR2 (NM_004560) Human 3' UTR Clone

Specifications

Product Data
Product Name	ROR2 (NM_004560) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	BDB; BDB1; NTRKR2
ACCN	NM_004560
Insert Size	1091 bp
Sequence Data	Insert Sequence (showhide) >SC212149 3’UTR clone of NM_004560 The sequence shown below is from the reference sequence of NM_004560. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GACGAGGCCCAAGTCCAGCTGGAAGCTTGAGTGGCACCAGGGCCCGGGGTTCGGGGATAGAAGCCCCGC CGAGACCCCACAGGGACCTCAGTCACCTTTGAGAAGACACCATACTCAGCAATCACAAGAGCCCGCCGG CCAGTGGGCTTGTTTGCAGACTGGGTGAGGTGGAGCCCTGCTCCTCTCTGTCCTCTGACACAGAGAGCT GCCCTGCCTAGGAGCACCCAAGCCAGGCAGGGGGTCTGGCAGCACGGCGTCCTGGGGAGCAGGACACAT GGTCATCCCCAGGGCTGTATACATTGATTCTGGTGGTAGACTGGTAGTGAGCAGCAAATGCCTTTCAAG AAAATAGGTGGCAGCTTCACTCCATGTCATATATGGAGTGAATATTTCAAAACGTTGGGAATAAGGGCC TGCAAAAGGCAGCGAGGAGGCACCTCGGGTCTTGAGGTTCCTGACAACCGATCTGGTCTGTTGGTTTGA GGATGAAGGGGCTCCATTTCTGCTGCCTCCCTGCTGAGAATATTCTCCCTTTAGCAGCCAAAGATTCGC TGGAACGGAGGCTGCCCTCTGCTGCCTGTTGGGGTCGGAAGACAAGGGGCTTCTGAAATGGGAGTTCCT GAGATACAACAAAATGTGTGCCTTCAAAGAAACTGACAGCTTTGTATTTGGTGAAATGGTTTTAATTAT ACTCCATGTGTATTTTGCCCACTTTTTTTGGGAATTCAAGGGAAAGTGTTTCTTGGGTTTGGAATGTTC AGAGGAAGCAGTATTGTACAGAACACGGTATTGTTATTTTTGTTAAGAATCATGTACAGAGCTTAAATG TAATTTATATGTTTTTAATATGCCATTTTCATTGAAGTATTTTGGTCTTAAGATGACTTTAGTAATTTA ACTGTTTATGTTACCCACGTTGGGATCCAGTTGGTCTTGGTTTGCTTCTCTCTGTACCACGTGCACATG AGGTCCATTCATTTTACAGCCCCTGTTACACACAGACCCACAGGCAGCCGTCTGTGCCCCGCACACATT GTTGGTCCTATTTGTAAATCCCACACCCGGTGTATCCAATAAAGTGAAACAAAGCA 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_004560.4
Synonyms	BDB; BDB1; NTRKR2
Summary	The protein encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance. [provided by RefSeq, Jul 2008]
Locus ID	4920
MW	40.6

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