Lmo4 (NM_010723) Mouse Untagged Clone

CAT#: MC207317

Lmo4 (untagged) - Mouse LIM domain only 4 (Lmo4), transcript variant 1, (10ug)


  "NM_010723" in other vectors (4)

Reconstitution Protocol

USD 420.00

3 Weeks*

Size
    • 10 ug

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Specifications

Product Data
Type Mouse Untagged Clone
Tag Tag Free
Symbol Lmo4
Synonyms A730077C12Rik; Crp3; Etohi4
Vector pCMV6-Entry
E. coli Selection Kanamycin (25 ug/mL)
Mammalian Cell Selection Neomycin
Sequence Data
>MC207317 representing NM_010723
Red=Cloning site Blue=ORF Orange=Stop codon

TTTTGTAATACGACTCACTATAGGGCGGCCGGGAATTCGTCGACTGGATCCGGTACCGAGGAGATCTGCC
GCCGCGATCGCC

ATGGTGAATCCGGGCAGCAGCTCGCAGCCGCCCCCGGTGACGGCCGGCTCCCTCTCCTGGAAGCGCTGCG
CAGGCTGCGGGGGCAAGATCGCGGACCGCTTTCTGCTCTATGCCATGGACAGCTACTGGCATAGCCGCTG
CCTCAAGTGCTCCTGCTGCCAGGCGCAGCTGGGCGACATTGGCACGTCCTGTTACACCAAGAGCGGCATG
ATCCTTTGCAGAAATGACTACATTAGGTTATTTGGGAATAGCGGTGCTTGCAGTGCCTGTGGACAGTCGA
TTCCTGCAAGTGAGCTCGTCATGAGGGCCCAAGGCAACGTGTATCATCTCAAGTGTTTCACATGTTCTAC
CTGCCGGAATCGCCTGGTCCCGGGAGATCGGTTTCACTACATCAATGGCAGTTTATTTTGTGAACATGAT
AGACCCACAGCCCTCATCAATGGCCATTTGAATTCACTTCAGAGCAATCCACTACTGCCAGACCAGAAGG
TCTGCTGA


ACGCGTACGCGGCCGCTCGAGCAGAAACTCATCTCAGAAGAGGATCTGGCAGCAAATGATATCCTGGATT
ACAAGGATGACGACGATAAGGTTTAA
Restriction Sites SgfI-MluI     
ACCN NM_010723
ORF Size 498 bp
Insert Size 498
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_010723.3, NP_034853.1
RefSeq Size 1704
RefSeq ORF 498
Locus ID 16911
Gene Summary Probable transcriptional factor. [UniProtKB/Swiss-Prot Function]
Transcript Variant: This variant (1) represents the longest transcript. Variants 1, 2 and 3 encode the same protein. 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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