CLC7 (CLCN7) (NM_001287) Human 3' UTR Clone

Specifications

Product Data
Product Name	CLC7 (CLCN7) (NM_001287) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CLC-7; CLC7; HOD; OPTA2; OPTB4; PPP1R63
ACCN	NM_001287
Insert Size	1726 bp
Sequence Data	Insert Sequence (showhide) >SC216069 3’UTR clone of NM_001287 The sequence shown below is from the reference sequence of NM_001287. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TTGGAGGAGCTCTCGCTGGCCCAGACGTGAGGCCCAGCCCTGCCCATAATGGGCACTGGCGCTGGCACC CCGGCCCTTCTGCATTTCCTCCCGGAGTCACTGGTTTCTCGGCCCAAACCATGCTCCCCAGCAGTGGCA ATGGCGAGCACCCTGCAGCTGGGCGGGCAGGCGGCAGGCGCGGAACTGACCCTCTCGCGGGACTGACCC TGTTGTGGGCAGTGGTCTCCCCCCTTGGCGCCTCCTTGCGCAGGCCCAGCCTCCACTCTCCTCGTCTAG GTTTCTTTACCTCCAGGGATCAGCTGTGTGTGTGTGACCTCCCTACCGGGCTATCGGCCTCTTGGGAGC CAGCGGCAGGGCCGGCACCTGCGTGCCTGTGCCCGTGTGCGTGAGACAGAGCCCTTGCCCCTGCTGCTG CCCCGAGGGCTGCCCTGCCCTGGAAGGGCCCCTCTGCCTCCACACCAGTGGAGTCTTCGAGACTTGGGA GCTGCTTGGCCTCATTTTCAGCCATGAGCAGACGGCCTGTGGTCCCTGGGCCTGAGGCACGGACTCGTA GCACCAGGGTTTGGAGGCTGCGACCGCCCCGGAGAGCAGCTTCACACTGGCGCCACAGAGGAGCCCCAC GTGCACTCCCCGGCCTGCATCCGGCTTGGGTACACAGGCCCAGAGGACTGGGGTGACTCACGGGCCCTG TGCTGTGATGTTGAGAGCTGAGAAAAACCTCCAAGGCCCTGAGCCCCATGCCCAGCCCTGCCTTGGTCC CCCAACCCCCAGAGCTTGGAGTCTGGGCCCCACACCCAGCCCTGCCTTGGTCCCTGAGCCTCAGAGCGT GGAATTGCTGCCCTGTGGACACTGGCTGGGAAGGCAGGTCTTCCCCTAGCACATGGGGACCCCGGCCTC GAGGGTGACCTCCCTACCCCGCCCCTGCCAGCCACCAAGCGCAGGTGCAGCGGGGGCCAGACTCCTGCC GGCCTCAGAGGACACCTGGCCCAGCACAGGCAGCTAGAAGGGCCGGTGGGCACCGGGGCCGGGAAGCCC CCACCTCACCACCTGAGGGCCCCTGGGAGGCTCCTCTGGCCTGGCTGGGCTGGGTCTGGGGCCGCCACA GGCCCCTCACGGGGCGGCAGAGGCAACTTCAGTGTCCCTGTTAGAGCAACACGGGTCCCTCCGTGGGGG GCTGGGTGCGGCCCCCTGCCGTGTATTTCCTCCCCAGGGAGTGGGGCCTCCCCGGGAGCTGACGCCACC ACCCTGCTTAGCCCTCACAGGGCCCCAAGGTGTCCGAGTGTGTTGGGTCTGAACGCGAAATAAAGAAAT CCTCTCAGCCCGCCTTTGCCAGCGTCGTCCCTCCCACCCCACCCAGACCACGTCCAACAGCCTGGGACT TTCGGGACCCTGGGGTCGGGGCACCGTGTGGAGTGAGAAAGGCGTGAAAGACAGCGGCTGCGGCCACCC AGGGCACCAGCCACATCCTCTTCCTCGTCCCCGCCCCTCAGCCTCCCTCCTCTGGCTCCTGGCTGGTGG GTCTGGGGGCAAGGCAGAGGCGCTCCAGGTGGAGGGGGGCGGGCCGGGGTGCCCACGCTGGGGTGACGC AAGAAGAAAACTCCCGGGCCTCAGAGTCGGCGCCGGAAACCTAGGTCTGGGTTTCCCTCGTGGTGGTTG TGTACTGAGGACCTGGAAGTGATCATATTTTGGATATATTCGGTTAAATAAAATCAGCGGTTAGGATTCA 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_001287.6
Synonyms	CLC-7; CLC7; HOD; OPTA2; OPTB4; PPP1R63
Summary	The product of this gene belongs to the CLC chloride channel family of proteins. Chloride channels play important roles in the plasma membrane and in intracellular organelles. This gene encodes chloride channel 7. Defects in this gene are the cause of osteopetrosis autosomal recessive type 4 (OPTB4), also called infantile malignant osteopetrosis type 2 as well as the cause of autosomal dominant osteopetrosis type 2 (OPTA2), also called autosomal dominant Albers-Schonberg disease or marble disease autosoml dominant. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. OPTA2 is the most common form of osteopetrosis, occurring in adolescence or adulthood. [provided by RefSeq, Jul 2008]
Locus ID	1186
MW	60.2

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