TRPV4 (NM_147204) Human Untagged Clone

CAT#: SC122052

TRPV4 (untagged)-Human transient receptor potential cation channel, subfamily V, member 4 (TRPV4), transcript variant 2


  "NM_147204" in other vectors (4)

Reconstitution Protocol

SC122052 is the updated version of SC121932.

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Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol TRPV4
Synonyms BCYM3; CMT2C; HMSN2C; OTRPC4; SMAL; SPSMA; SSQTL1; TRP12; VRL2; VROAC
Vector pCMV6-XL4
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF within SC122052 sequence for NM_147204 edited (data generated by NextGen Sequencing)
ATGGCGGATTCCAGCGAAGGCCCCCGCGCGGGGCCCGGGGAGGTGGCTGAGCTCCCCGGG
GATGAGAGTGGCACCCCAGGTGGGGAGGCTTTTCCTCTCTCCTCCCTGGCCAATCTGTTT
GAGGGGGAGGATGGCTCCCTTTCGCCCTCACCGGCTGATGCCAGTCGCCCTGCTGGCCCA
GGCGATGGGCGACCAAATCTGCGCATGAAGTTCCAGGGCGCCTTCCGCAAGGGGGTGCCC
AACCCCATCGATCTGCTGGAGTCCACCCTATATGAGTCCTCGGTGGTGCCTGGGCCCAAG
AAAGCACCCATGGACTCACTGTTTGACTACGGCACCTATCGTCACCACTCCAGTGACAAC
AAGAGGTGGAGGAAGAAGATCATAGAGAAGCAGCCGCAGAGCCCCAAAGCCCCTGCCCCT
CAGCCGCCCCCCATCCTCAAAGTCTTCAACCGGCCTATCCTCTTTGACATCGTGTCCCGG
GGCTCCACTGCTGACCTGGACGGGCTGCTCCCATTCTTGCTGACCCACAAGAAACGCCTA
ACTGATGAGGAGTTTCGAGAGCCATCTACGGGGAAGACCTGCCTGCCCAAGGCCTTGCTG
AACCTGAGCAATGGCCGCAACGACACCATCCCTGTGCTGCTGGACATCGCGGAGCGCACC
GGCAACATGCGGGAGTTCATTAACTCGCCCTTCCGTGACATCTACTATCGAGGTCAGACA
GCCCTGCACATCGCCATTGAGCGTCGCTGCAAACACTACGTGGAACTTCTCGTGGCCCAG
GGAGCTGATGTCCACGCCCAGGCCCGTGGGCGCTTCTTCCAGCCCAAGGATGAGGGGGGC
TACTTCTACTTTGGGGAGCTGCCCCTGTCGCTGGCTGCCTGCACCAACCAGCCCCACATT
GTCAACTACCTGACGGAGAACCCCCACAAGAAGGCGGACATGCGGCGCCAGGACTCGCGA
GGCAACACAGTGCTGCATGCGCTGGTGGCCATTGCTGACAACACCCGTGAGAACACCAAG
TTTGTTACCAAGATGTACGACCTGCTGCTGCTCAAGTGTGCCCGCCTCTTCCCCGACAGC
AACCTGGAGGCCGTGCTCAACAACGACGGCCTCTCGCCCCTCATGATGGCTGCCAAGACG
GGCAAGATTGGGAACCGCCACGAGATGCTGGCTGTGGAGCCCATCAATGAACTGCTGCGG
GACAAGTGGCGCAAGTTCGGGGCCGTCTCCTTCTACATCAACGTGGTCTCCTACCTGTGT
GCCATGGTCATCTTCACTCTCACCGCCTACTACCAGCCGCTGGAGGGCACACCGCCGTAC
CCTTACCGCACCACGGTGGACTACCTGCGGCTGGCTGGCGAGGTCATTACGCTCTTCACT
GGGGTCCTGTTCTTCTTCACCAACATCAAAGACTTGTTCATGAAGAAATGCCCTGGAGTG
AATTCTCTCTTCATTGATGGCTCCTTCCAGCTGCTCTACTTCATCTACTCTGTCCTGGTG
ATCGTCTCAGCAGCCCTCTACCTGGCAGGGATCGAGGCCTACCTGGCCGTGATGGTCTTT
GCCCTGGTCCTGGGCTGGATGAATGCCCTTTACTTCACCCGTGGGCTGAAGCTGACGGGG
ACCTATAGCATCATGATCCAGAAGATTCTCTTCAAGGACCTTTTCCGATTCCTGCTCGTC
TACTTGCTCTTCATGATCGGCTACGCTTCAGCCCTGGTCTCCCTCCTGAACCCGTGTGCC
AACATGAAGGTGTGCAATGAGGACCAGACCAACTGCACAGTGCCCACTTACCCCTCGTGC
CGTGACAGCGAGACCTTCAGCACCTTCCTCCTGGACCTGTTTAAGCTGACCATCGGCATG
GGCGACCTGGAGATGCTGAGCAGCACCAAGTACCCCGTGGTCTTCATCATCCTGCTGGTG
ACCTACATCATCCTCACCTTTGTGCTGCTCCTCAACATGCTCATTGCCCTCATGGGCGAG
ACAGTGGGCCAGGTCTCCAAGGAGAGCAAGCACATCTGGAAGCTGCAGTGGGCCACCACC
ATCCTGGACATTGAGCGCTCCTTCCCCGTATTCCTGAGGAAGGCCTTCCGCTCTGGGGAG
ATGGTCACCGTGGGCAAGAGCTCGGACGGCACTCCTGACCGCAGGTGGTGCTTCAGGGTG
GATGAGGTGAACTGGTCTCACTGGAACCAGAACTTGGGCATCATCAACGAGGACCCGGGC
AAGAATGAGACCTACCAGTATTATGGCTTCTCGCATACCGTGGGCCGCCTCCGCAGGGAT
CGCTGGTCCTCGGTGGTACCCCGCGTGGTGGAACTGAACAAGAACTCGAACCCGGACGAG
GTGGTGGTGCCTCTGGACAGCATGGGGAACCCCCGCTGCGATGGCCACCAGCAGGGTTAC
CCCCGCAAGTGGAGGACTGATGACGCCCCGCTCTAG

Clone variation with respect to NM_147204.2
670 a=>c
>OriGene 5' read for NM_147204 unedited
GATATTTGTAATCACGACTTCACTATAGGGCGGCACGCGCAATTCGGCACGAGGTACCCT
GGTACTCCATCACTAACCTGCTGTGTGACCTCAGGCTGAGCAGTGCAGACGGGCCTGGGG
CAGGCATGGCGGATTCCAGCGAAGGCCCCCGCGCGGGGCCCGGGGAGGTGGCTGAGCTCC
CCGGGGATGAGAGTGGCACCCCAGGTGGGGAGGCTTTTCCTCTCTCCTCCCTGGCCAATC
TGTTTGAGGGGGAGGATGGCTCCCTTTCGCCCTCACCGGCTGATGCCAGTCGCCCTGCTG
GCCCAGGCGATGGGCGACCAAATCTGCGCATGAAGTTCCAGGGCGCCTTCCGCAAGGGGG
TGCCCAACCCCATCGATCTGCTGGAGTCCACCCTATATGAGTCCTCGGTGGTGCCTGGGC
CCAAGAAAGCACCCATGGACTCACTGTTTGACTACGGCACCTATCGTCACCACTCCAGTG
ACAACAAGAGGTGGAGGAAGAAGATCATAGAGAAGCAGCCGCAGAGCCCCAAAGCCCCTG
CCCCTCAGCCGCCCCCCATCCTCAAAGTCTTCAACCGGCCTATCCTCTTTGACATCGTGT
CCCGGNGCTCCACTGCTGACCTGGACGGGCTGCTCCCATTCTTGCTGACCCANCAGAAAC
GCCTAACTGATGANGAGTTNCGAGAGCCATCTACGGGGAAGACCTGCCTGCCCAAGGCCT
TTGCTGACCTGAGCAATGGCCGCNACGACACCATCCCNTGTGCTGCTGGACATCGCGNAG
CGCCACGGGCACATGCNGGAGTTCATTACTCGCCCTTTCGTGACTCTACTTTCGAGTCAG
ACAGCCCTGCCATCGCCATGAACGTCGCTGCAACACTACGTGGAACTTCTCGTGCCCAGG
AAGCTGATGTCCACGCCAAGCCCTGGGCGCCTTTTCCACCCCAGGTGAAGGGGGCTACCT
CTACTTTGGNACCTGCCCCTGTCCTT
>OriGene 3' read for NM_147204 unedited
TTACTTTGGACNCGCGGCCGCAATCTANGATCGAGTTTTTTTTTTTTTTTTTTCAATGAA
TAAACATTTATTGAGCACCGGCAAATCCCAGACACTACAGAACACACAGAAGGCATGGCC
CCACGCCGAGGGCCCCAGCCCCTTGCAAAGCTGCCACGCTGCCAAAAATGGTGGCGCATG
CAGCTCAGGCGCAGGCTGAGGCTGGGGCTTGGCCGGGCAGTGCACTTGGAACGGGGTCCT
AAGGCCTCTGCCAGGTTCCAGCTGGGGCAGGGGTCACGTCGCTTCCTGAGAGCAGAGCAA
ATAAATAATGGAGAGGCAGGGGCTGGGGCCTGAGGTGGAGGGGCTCTGGCGTTGGCTTAT
GTGACTCCATAGGAGCAAGACAGGTGGCCGGGAGCCCCCACCCCAGGGTGGGGAGGCAGA
GCCACGGGACCACAGGGTCCTGGGGCCTCCCTGGCACCTCCACTGGTCCCTCGCCTCTGG
GGCCAAAGCAGGGTGTGGGGGGACACCCCAGAAGGCACTGCTGAAATGCGGCTGGACTAG
AAATGAGTGGGCAGAGAAGCTGGGGCTGGGCTGCAGTCCCTAGAGCGGGGCGTCATCAGT
CCTCCACTTGCGGGGGTAACCCTGCTGGTGGCCATCGCAGCGGGGGTTCCCCATGCTGTC
CAGAGGCACCACCACCTCGTCCGGGTTCGAGTTCTTGTTCAGTTCCACCACGCGGNGTAC
CACCGAGGACCAGCGATCCCTGCGGAGGCGGCCCACGGTATGCGAGAAGCCATAATACTG
GTAGGTCTCATTCTTGCCCGGGTCCTCGTTGATGATGCCCAAGTTCTGGTTCCAGTGAGA
CCAGTTCACCTCATCCACCCTGAAGCACACCTGTCGTCAGAAGTGCCGTCCGAGCTTTGC
CCACGGTGACATCTCCCAGACGGAAGCCTTCTCAGAATACGGGAAGAGCGT
Restriction Sites NotI-NotI     
ACCN NM_147204
ORF Size 2436 bp
Insert Size 3150
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_147204.1, NP_671737.1
RefSeq Size 3057
RefSeq ORF 2436
Locus ID 59341
Protein Families Druggable Genome, Ion Channels: Transient receptor potential, Transmembrane
Gene Summary This gene encodes a member of the OSM9-like transient receptor potential channel (OTRPC) subfamily in the transient receptor potential (TRP) superfamily of ion channels. The encoded protein is a Ca2+-permeable, nonselective cation channel that is thought to be involved in the regulation of systemic osmotic pressure. Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2010]
Transcript Variant: This variant (2) lacks an alternate in-frame exon compared to variant 1, resulting in an isoform (b) that lacks an internal segment compared to isoform a.

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