Cuta (NM_212494) Rat Untagged Clone

CAT#: RN213977

Cuta (untagged ORF) - Rat cutA divalent cation tolerance homolog (E. coli) (Cuta), (10 ug)


  "NM_212494" in other vectors (3)

Reconstitution Protocol

USD 420.00

4 Weeks*

Size
    • 10 ug

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Specifications

Product Data
Type Rat Untagged Clone
Tag Tag Free
Symbol Cuta
Synonyms CutA1
Vector pCMV6-Entry
E. coli Selection Kanamycin (25 ug/mL)
Mammalian Cell Selection Neomycin
Sequence Data
>RN213977 representing NM_212494
Red=Cloning site Blue=ORF Orange=Stop codon

TTTTGTAATACGACTCACTATAGGGCGGCCGGGAATTCGTCGACTGGATCCGGTACCGAGGAGATCTGCC
GCCGCGATCGCC

ATGAACTGGGGGCGGGCGCTCGGCGTCCTACTCGGCGGAGGGGCCACGCTGCTCCTGTCGTTTCTTTGCA
TGCCTGCCCTACTGCCGGTGGCTTCCCGCCTTCTATTGCTACCCCGAGCTCTGCTGTCCATGGCTTCTGG
AAGCCCTCCGTCCCAGCCGTCGCCGGCCTCGGGCTCCGGCTACGTTCCAGGATCAGTCTCTGCAGCCTTT
GTCACTTGTCCGAACGAAAAAGTCGCCAAGGAGATTGCCAGGGCAGTGGTAGAGAAGCGCCTGGCAGCCT
GCGTCAACCTCATCCCGCAGATCACATCCATCTATGAATGGAAAGGAAAGATCGAGGAAGATAGTGAGGT
GCTGATGATGATTAAAACACAAAGCTCCCTGGTCCCTGCTCTGACAGAGTTTGTCCGATCTGTGCACCCT
TATGAAGTTGCCGAGGTGATCGCACTGCCCGTGGAGCAGGGGAATCCCCCGTATCTGCACTGGGTGCACC
AGGTCACGGAATCAGTGTCAGGCTCTGGCAAGGCCCTACCATGA


ACGCGTACGCGGCCGCTCGAGCAGAAACTCATCTCAGAAGAGGATCTGGCAGCAAATGATATCCTGGATT
ACAAGGATGACGACGATAAGGTTTAA
Restriction Sites SgfI-MluI     
ACCN NM_212494
ORF Size 534 bp
Insert Size 534
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_212494.2, NP_997659.2
RefSeq Size 718
RefSeq ORF 534
Locus ID 294288
Gene Summary may play a role in anchoring acetylcholinesterase in neuronal cell membranes; may be involved in signal transduction [RGD, Feb 2006]
Transcript Variant: This variant (1) encodes the longer isoform (1). Sequence Note: The RefSeq transcript and protein were derived from genomic sequence. The genomic coordinates used for the transcript record were based on alignments.

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