CECR2 (NM_001290047) Human Untagged Clone

CAT#: SC338053

CECR2 (untagged) - Human cat eye syndrome chromosome region, candidate 2 (CECR2), transcript variant 1


  "NM_001290047" in other vectors (1)

Reconstitution Protocol

USD 1,480.00

5 Weeks*

Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol CECR2
Vector pCMV6-Entry
E. coli Selection Kanamycin (25 ug/mL)
Mammalian Cell Selection Neomycin
Sequence Data
>NCBI ORF sequence for NM_001290047, the custom clone sequence may differ by one or more nucleotides


ATGTGCCCAGAGGAGGGCGGCGCGGCCGGGCTGGGCGAGCTCCGCTCCTGGTGGGAGGTCCCGGCCATCG
CGCACTTCTGCTCGCTCTTTCGCACCGCGTTCCGCCTGCCCGACTTCGAGATCGAGGAGTTAGAAGCCGC
TCTTCACAGAGATGACGTGGAGTTTATCAGTGACCTGATTGCCTGCCTGCTTCAGGGCTGCTATCAACGA
AGAGATATCACGCCTCAGACATTCCACAGCTACCTAGAGGACATCATCAACTACCGCTGGGAGCTCGAAG
AAGGGAAGCCCAACCCTCTGAGGGAAGCCAGTTTCCAGGACCTGCCTCTTCGCACACGGGTGGAGATCCT
GCACCGACTCTGTGATTACCGGCTGGATGCAGACGATGTCTTCGATCTTCTAAAGGGCCTGGATGCAGAC
AGTCTCCGTGTGGAGCCATTGGGTGAAGACAATTCTGGGGCACTATATTGGTATTTCTATGGAACACGAA
TGTACAAAGAGGACCCGGTGCAAGGAAAATCCAATGGAGAACTCTCTTTGAGCAGGGAAAGTGAAGGACA
AAAAAATGTCTCAAGTATTCCTGGAAAAACGGGAAAAAGAAGAGGAAGACCCCCAAAACGGAAGAAACTG
CAGGAGGAGATTCTGTTGAGTGAAAAGCAGGAAGAAAATTCCTTGGCATCCGAGCCACAGACAAGACATG
GGTCCCAAGGGCCAGGCCAAGGTACTTGGTGGCTCCTGTGCCAGACAGAAGAGGAATGGAGACAGGTCAC
CGAGAGTTTTCGCGAGAGGACCTCCCTTCGAGAACGGCAGCTCTACAAGCTCCTCAGTGAGGACTTCCTG
CCTGAGATCTGCAACATGATCGCCCAGAAGGGAAAACGTCCACAGCGCACAAAGGCAGAGTTGCATCCTA
GGTGGATGTCTGACCACCTGTCCATCAAACCCGTCAAGCAAGAGGAGACTCCTGTGCTGACCAGAATAGA
AAAACAAAAGCGCAAAGAGGAGGAAGAAGAGCGTCAGATTCTTCTAGCAGTGCAGAAGAAGGAGCAGGAG
CAGATGCTAAAGGAAGAGAGGAAACGCGAGTTGGAGGAGAAGGTCAAGGCAGTGGAAGATCGAGCGAAGA
GGAGAAAGCTCAGGGAAGAAAGGGCATGGCTGCTGGCTCAAGGAAAGGAGCTCCCTCCAGAACTTTCCCA
TCTGGACCCCAATTCCCCCATGAGAGAGGAAAAAAAGACTAAAGACCTCTTTGAGTTGGATGATGATTTC
ACTGCTATGTATAAAGTTCTAGACGTGGTAAAGGCTCACAAGGATTCCTGGCCCTTCTTGGAACCTGTGG
ATGAATCTTATGCCCCTAACTATTATCAGATTATTAAGGCCCCCATGGATATTTCCAGCATGGAGAAGAA
ACTGAATGGAGGTTTATACTGTACCAAGGAGGAATTTGTAAATGACATGAAGACCATGTTCAGGAATTGT
CGAAAGTATAATGGGGAAAGTAGTGAGTATACCAAGATGTCTGATAATTTAGAGAGGTGTTTCCATCGGG
CAATGATGAAACATTTTCCTGGAGAAGATGGAGACACAGATGAAGAATTTTGGATTCGAGAGGATGAAAA
GCGGGAGAAAAGACGGAGTCGGGCTGGGCGAAGTGGTGGGAGCCATGTTTGGACCCGCTCCAGGGACCCA
GAAGGGTCCAGCAGGAAACAGCAGCCCATGGAGAATGGAGGAAAGTCGTTGCCCCCCACACGCCGAGCGC
CCTCTTCTGGGGACGATCAGAGCAGCAGCTCCACACAGCCCCCGCGGGAGGTGGGCACTTCCAATGGCCG
AGGTTTTTCTCATCCCCTGCATTGTGGTGGGACACCCAGCCAGGCACCCTTTTTAAACCAGATGAGGCCA
GCAGTACCAGGAACATTTGGCCCTCTGCGAGGATCAGATCCTGCCACCTTGTATGGCTCCTCTGGAGTCC
CGGAGCCACACCCCGGGGAGCCTGTGCAGCAGCGTCAGCCTTTCACCATGCAGCCTCCAGTTGGAATTAA
CAGCCTCCGAGGACCCAGGCTAGGCACACCAGAGGAGAAGCAAATGTGCGGGGGGCTGACACACCTTTCT
AACATGGGCCCACACCCTGGATCCTTGCAGCTTGGGCAGATAAGTGGCCCAAGTCAGGATGGAAGCATGT
ATGCTCCAGCTCAGTTCCAGCCAGGATTCATTCCTCCCCGGCATGGGGGGGCTCCAGCCCGGCCACCAGA
CTTTCCTGAAAGCTCAGAAATTCCTCCCAGCCATATGTATCGATCGTACAAGTACCTGAATCGAGTACAC
TCTGCCGTCTGGAATGGGAACCATGGTGCTACGAACCAAGGACCCTTGGGCCCAGATGAGAAGCCCCACC
TGGGGCCAGGACCCTCTCACCAGCCTCGCACTCTCGGTCACGTGATGGATTCCCGAGTCATGAGACCACC
TGTCCCCCCCAACCAGTGGACTGAACAATCAGGCTTCCTACCTCATGGAGTTCCTTCCTCAGGGTACATG
CGACCGCCCTGCAAGTCTGCCGGACATCGGTTACAGCCACCTCCAGTGCCAGCACCCAGTTCTTTGTTTG
GAGCACCTGCCCAGGCTCTTCGGGGGGTGCAGGGAGGGGACTCCATGATGGACAGCCCAGAGATGATTGC
GATGCAGCAGCTCTCCTCCCGCGTCTGCCCCCCAGGTGTGCCTTACCACCCCCACCAGCCTGCACACCCC
CGTTTACCTGGCCCTTTTCCGCAGGTAGCTCACCCAATGTCAGTCACTGTGTCAGCCCCCAAGCCTGCCC
TGGGCAACCCTGGGAGGGCACCGGAGAACAGTGAAGCACAAGAGCCTGAGAATGACCAAGCAGAGCCGTT
GCCTGGCCTTGAAGAGAAACCACCAGGTGTTGGTACTTCAGAGGGGGTCTACCTCACACAACTACCTCAC
CCCACACCTCCCCTGCAGACTGACTGCACCAGGCAGAGCTCACCACAAGAAAGGGAAACAGTGGGCCCGG
AGCTCAAAAGCAGCTCCTCCGAATCTGCGGACAACTGTAAAGCAATGAAGGGCAAGAATCCCTGGCCCTC
GGATAGCAGCTACCCCGGCCCAGCCGCCCAAGGGTGCGTGAGAGACCTCTCCACGGTGGCAGACAGGGGC
GCTCTATCCGAGAACGGAGTCATTGGGGAAGCATCTCCTTGTGGATCGGAGGGGAAGGGCCTTGGTAGCA
GTGGTTCCGAAAAGCTGCTCTGCCCCAGAGGCAGAACGTTGCAGGAAACCATGCCATGCACGGGACAGAA
CGCAGCGACACCGCCCAGCACAGACCCCGGTTTGACGGGAGGCACTGTGAGCCAGTTTCCCCCGCTGTAT
ATGCCTGGCCTAGAGTACCCGAATTCAGCTGCCCATTACCACATCAGTCCAGGCCTGCAGGGTGTGGGCC
CTGTGATGGGAGGGAAGTCCCCAGCATCCCATCCCCAGCATTTTCCCCCAAGGGGCTTTCAGTCTAACCA
CCCACATTCTGGAGGCTTTCCCCGGTATCGCCCCCCACAAGGAATGAGGTATTCCTACCACCCACCGCCA
CAGCCTTCCTACCACCACTATCAGCGAACTCCTTACTATGCCTGTCCACAGAGCTTTTCTGACTGGCAGA
GACCTCTCCATCCCCAGGGAAGCCCAAGCGGACCCCCAGCCAGTCAGCCTCCCCCACCAAGGTCCCTCTT
CTCAGATAAGAATGCCATGGCCAGTCTGCAAGGCTGTGAGACACTGAATGCTGCCTTAACTTCTCCAACC
CGTATGGATGCAGTGGCTGCTAAAGTCCCAAATGACGGGCAGAATCCTGGTCCAGAGGAAGAGAAGCTGG
ATGAATCTATGGAGAGGCCAGAGAGTCCCAAAGAATTTTTAGACCTGGACAACCATAACGCAGCTACCAA
GCGGCAGAGCTCGTTGTCAGCCAGCGAGTATCTCTATGGAACTCCTCCGCCTCTGAGTTCAGGAATGGGA
TTTGGTTCATCTGCATTTCCACCCCACAGTGTGATGCTGCAGACGGGGCCTCCCTATACCCCTCAGCGGC
CGGCCAGTCACTTTCAGCCCAGGGCTTACTCTTCCCCTGTGGCTGCCCTCCCACCTCACCACCCAGGGGC
CACCCAGCCCAACGGCCTCTCTCAGGAGGGTCCCATCTATCGCTGCCAGGAAGAAGGCCTGGGTCACTTT
CAAGCTGTGATGATGGAACAAATTGGCACTAGAAGTGGAATAAGAGGACCTTTCCAGGAAATGTACAGAC
CATCAGGAATGCAGATGCACCCGGTCCAGTCGCAGGCCTCGTTCCCAAAGACCCCCACAGCAGCAACATC
ACAGGAGGAGGTGCCGCCTCATAAGCCTCCAACACTTCCCCTGGATCAGAGCTAG


Restriction Sites SgfI-MluI     
ACCN NM_001290047
ORF Size 4395 bp
OTI Disclaimer Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
Reference Data
RefSeq NM_001290047.1, NP_001276976.1
RefSeq Size 10128
RefSeq ORF 4395
Locus ID 27443
Gene Summary This gene encodes a bromodomain-containing protein that is involved in chromatin remodeling, and may additionally play a role in DNA damage response. The encoded protein functions as part of an ATP-dependent complex that is involved in neurulation. This gene is a candidate gene for Cat Eye Syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]
Transcript Variant: This variant (1) represents the longer transcript and encodes the longer isoform (1). Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.

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