DNAL1 (NM_031427) Human Untagged Clone

CAT#: SC320816

DNAL1 (untagged)-Human dynein, axonemal, light chain 1 (DNAL1), transcript variant 1


  "NM_031427" in other vectors (6)

Reconstitution Protocol

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Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol DNAL1
Synonyms C14orf168; CILD16; LC1
Vector pCMV6-AC
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection Neomycin
Sequence Data
>OriGene sequence for NM_031427.1 GGGCCCTAGCAACCAGAGCAGTGACAGTAGCAACCGCCGGAATGGCGAAAGCAACAACAA
TCAAAGAAGCCTTAGCGAGATGGGAAGAGAAAACTGGCCAGAGGCCATCTGAAGCCAAAG
AGATAAAACTTTATGCCCAGATTCCCCCTATAGAGAAGATGGATGCATCCTTGTCCATGC
TTGCTAATTGCGAGAAGCTTTCACTGTCTACAAACTGCATTGAAAAAATTGCCAACCTGA
ATGGCTTAAAAAACTTGAGGATATTATCTTTAGGAAGAAACAACATAAAGAACTTAAATG
GACTGGAGGCAGTAGGGGACACATTAGAAGAACTGTGGATCTCCTACAATTTTATTGAGA
AGTTGAAAGGGATCCACATAATGAAGAAATTGAAGATTCTCTACATGTCTAATAACCTGG
TAAAAGACTGGGCTGAGTTTGTGAAGCTGGCAGAACTGCCATGCCTCGAAGACCTGGTGT
TTGTAGGCAATCCCTTGGAAGAGAAACATTCTGCTGAGAATAACTGGATTGAAGAAGCAA
CCAAGAGAGTGCCCAAACTGAAAAAGCTGGATGGTACTCCAGTAATTAAAGGGGATGAGG
AAGAAGACAACTAATGCCACGCTTTCCACTGTGTGTTAACTTATTTAAATGTCATAAGAA
CAATAGATAAATTTTATATAATTGTCTATTTTAAAGATTCTGTATGGGACAAAAGTTTCT
TAAGATAAAACAGATCACTCATTCTCATCTTTTTTTTTCCTTTAACTTATTCAGTGTTTC
TCCCCAAAACTGGTAATGCCAACCTTATATATCGTATTTCTCTTTTTAGAAACCACAAAT
TTTCGATTTTTGTCTTCAGTCTCAGTTACGTACTGTGTAGCCCCATCTACTAAAACAAAA
CCTTTGTAGACCAGTCATTTTTAATAACAAAGGAACAAATGTTTTTTTCAGTTTGTTCAT
TTTTTTTTAGGTTAGACATTTTAAAAGATGTACATTTGAAAATTCAGAACATTTTTCCTG
AAGGTCTGTCTCTGTACAATTCAGAAGCACATGCCTTTAGCTCAGAAGGCAGCATGGTGA
TGGGAAGAGTTCCTCTTAGAAATACAGCAGGTCCGGAACCAAGACTCCAAAGTTCCATTG
GAAAAGATATGGTGAAAAAAGGAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
>OriGene 5' read for NM_031427.1 unedited
TCATTTGTATACGACTCCTATAGGGCGGCTCGGGTAATTCGGCCATTACGGCCGGGGGGG
CCCTAGCAACCAGAGCAGTGACAGCTAGCAACCGCCGGAATGGCGAAAGCAACAACAATC
AAAGAAGCCTTAGCGAGATGGGAAGAGAAAACTGGCCAGAGGCCATCTGAAGCCAAAGAG
ATAAAACTTTATGCCCAGATTCCCCCTATAGAGAAGATGGATGCATCCTTGTCCATGCTT
GCTAATTGCGAGAAGCTTTCACTGTCTACAAACTGCATTGAAAAAATTGCCAACCTGAAT
GGCTTAAAAAACTTGAGGATATTATCTTTAGGAAGAAACAACATAAAGAACTTAAATGGA
CTGGAGGCAGTAGGGGACACATTAGAAGAACTGTGGATCTCCTACAATTTTATTGAGAAG
TTGAAAGGGATCCACATAATGAAGAAATTGAAGATTCTCTACATGTCTAATAACCTGGTA
AAAGACTGGGCTGAGTTTGTGAAGCTGGCAGAACTGCCATGCCTCGAAGACCTGGTGTTT
GTAGGCAATCCCTTGGAAGAGAAACATTCTGCTGAGAATAACTGGATTGAAGAAGCAACC
AAGAGAGTGCCCAAACTGAAAAAGCTGGATGGTACTCCAGTAATTAAAGGGGATGAGGAA
GAAGACAACTAATGCCACGCTTTCCACTGTGTGTTAACTTATTTAAATGTCATAAGACAA
TAGATAAATTTTATATAATTGTCTATTTTAAAGATTCTGTATGGGACAAAAGTTTCTTAA
GATAAAACAGATCACTCATCTCATCTTTTTTTTCCTTTAACTTATTCAGTGTTTCTCCCA
AACTGTAATGCCGACCTTATATATCGTATTCTCTTTTAGAAACCACAAATTTCGATTTTT
GTCTTCAGTCTCAGTACGTACTGGGGTAGCCCCATTCTACTAAAACAAAAAC
Restriction Sites Please inquire     
ACCN NM_031427
ORF Size 456 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_031427.1, NP_113615.1
RefSeq Size 1191
RefSeq ORF 456
Locus ID 83544
Domains LRR, LRR_SD22
Protein Pathways Huntington's disease
Gene Summary This gene encodes an axonemal dynein light chain which functions as a component of the outer dynein arms complex. This complex acts as the molecular motor that provides the force to move cilia in an ATP-dependent manner. The encoded protein is expressed in tissues with motile cilia or flagella and may be involved in the movement of sperm flagella. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2011]
Transcript Variant: This variant (1) 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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