Lebercilin (LCA5) (NM_001122769) Human Untagged Clone

CAT#: SC318970

LCA5 (untagged)-Human Leber congenital amaurosis 5 (LCA5), transcript variant 2


  "NM_001122769" in other vectors (4)

Reconstitution Protocol

USD 760.00

3 Weeks*

Size
    • 10 ug

Product Images

Other products for "LCA5"

Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol LCA5
Synonyms C6orf152
Vector pCMV6-Entry
E. coli Selection Kanamycin (25 ug/mL)
Mammalian Cell Selection Neomycin
Sequence Data
>NCBI ORF sequence for NM_001122769, the custom clone sequence may differ by one or more nucleotides


ATGGGGGAAAGAGCAGGAAGTCCAGGTACTGATCAAGAAAGAAAGGCAGGCAAACACCATTATTCTTACT
TATCTGATTTTGAAACGCCACAGTCTTCTGGCCGATCATCGCTGGTCAGTTCTTCACCTGCAAGTGTTAG
GAGAAAAAATCCTAAAAGACAAACTTCAGATGGCCAAGTACATCACCAAGCCCCTCGGAAACCAAGCCCT
AAGGGTCTACCAAACAGAAAGGGAGTCCGAGTGGGATTTCGCTCCCAGAGCCTCAATAGAGAGCCACTTC
GGAAAGATACTGATCTTGTTACAAAACGGATTCTGTCTGCAAGACTGCTAAAAATCAATGAGTTGCAGAA
TGAAGTATCTGAACTCCAGGTCAAGTTAGCTGAGCTGCTAAAAGAAAATAAATCTTTGAAAAGGCTTCAG
TACAGACAGGAGAAAGCCCTGAATAAGTTTGAAGATGCCGAAAATGAAATCTCACAACTTATATTTCGTC
ATAACAATGAGATTACAGCACTCAAAGAACGCTTAAGAAAATCTCAAGAGAAAGAACGGGCAACTGAGAA
AAGGGTAAAAGATACAGAAAGTGAACTATTTAGGACAAAATTTTCCTTACAGAAACTGAAAGAGATCTCT
GAAGCTAGACACCTACCTGAACGAGATGATTTGGCAAAGAAACTAGTTTCAGCAGAGTTAAAGTTAGATG
ACACCGAGAGAAGAATTAAGGAGCTATCGAAAAACCTTGAACTGAGTACTAACAGTTTCCAACGACAGTT
GCTTGCTGAAAGGAAAAGGGCATATGAGGCTCATGATGAAAATAAAGTTCTTCAAAAGGAGGTACAGCGA
CTATATCACAAATTAAAGGAAAAGGAGAGAGAACTGGATATAAAAAATATATATTCTAATCGTCTGCCAA
AGTCCTCTCCAAATAAAGAGAAAGAACTTGCATTAAGAAAAAATGCTGCATGCCAGAGTGATTTTGCAGA
CCTGTGTACAAAAGGAGTACAAACCATGGAAGACTTCAAGCCAGAAGAATATCCTTTAACTCCAGAAACA
ATTATGTGTTACGAAAACAAATGGGAAGAACCAGGACATCTTACTTTGGACTTGCAATCTCAAAAGCAAG
ACAGGCATGGAGAAGCAGGGATTCTAAACCCAATTATGGAAAGAGAAGAAAAATTTGTTACAGATGAAGA
ACTCCATGTCGTAAAACAGGAGGTTGAAAAGCTGGAGGATGAATGGGAAAGAGAAGAACTTGATAAAAAG
CAAAAAGAAAAGGCATCTTTACTGGAAAGAGAAGAAAAGCCAGAGTGGGAAACTGGAAGGTACCAACTAG
GAATGTATCCAATTCAGAATATGGATAAATTGCAAGGAGAGGAAGAAGAAAGACTGAAGAGAGAAATGCT
ACTTGCTAAACTGAATGAAATTGACAGAGAACTCCAAGATTCTCGAAATCTAAAATACCCTGTTTTGCCA
TTGTTACCTGATTTTGAATCAAAACTACACTCCCCAGAGAGAAGCCCCAAAACATACAGGTTCTCTGAAT
CCTCAGAGAGATTATTTAATGGGCATCATTTGCAAGACATCAGTTTCTCAACTCCAAAAGGAGAAGGTCA
GAATTCAGGAAATGTTAGAAGTCCAGCCTCCCCTAATGAGTTCGCATTTGGTAGCTACGTGCCTTCGTTT
GCAAAAACATCAGAGAGGTCAAATCCATTTAGTCAAAAAAGTAGTTTTTTGGATTTCCAAAGAAACAGTA
TGGAAAAACTTAGTAAAGATGGTGTAGATTTAATTACAAGAAAAGAGAAAAAAGCTAATTTGATGGAACA
GTTATTTGGTGCCAGTGGTAGCAGCACCATTTCCTCCAAAAGCAGTGACCCAAATTCTGTGGCTTCCAGT
AAAGGAGACATTGACCCTCTAAATTTTCTCCCTGGGAATAAAGGCAGCAGAGATCAAGAACATGATGAAG
ATGAAGGCTTTTTCCTCAGTGAAGGAAGAAGTTTTAATCCAAATAGGCACCGATTAAAACATGCAGACGA
TAAACCAGCAGTAAAAGCAGCTGATTCTGTAGAAGATGAAATTGAAGAAGTAGCACTGAGATGA


Restriction Sites SgfI-MluI     
ACCN NM_001122769
ORF Size 2094 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).
OTI Annotation This TrueClone is provided through our Custom Cloning Process that includes sub-cloning into OriGene's pCMV6 vector and full sequencing to provide a non-variant match to the expected reference without frameshifts, and is delivered as lyophilized plasmid DNA.
Reference Data
RefSeq NM_001122769.2, NP_001116241.1
RefSeq Size 4574
RefSeq ORF 2094
Locus ID 167691
Gene Summary This gene encodes a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. Alternatively spliced transcript variants are described. [provided by RefSeq, Oct 2009]
Transcript Variant: This variant (2) differs in the 5' UTR compared to variant 1. Both variants 1 and 2 encode the same protein.

Other Versions

{0} Product Review(s)

0 Product Review(s) Submit review

Be the first one to submit a review

Product Citations

*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.