PHD finger protein 6 (PHF6) (NM_032335) Human Untagged Clone

CAT#: SC319341

PHF6 (untagged)-Human PHD finger protein 6 (PHF6), transcript variant 3


  "NM_032335" in other vectors (4)

Reconstitution Protocol

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Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol PHF6
Synonyms BFLS; BORJ; CENP-31
Vector pCMV6-AC
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection Neomycin
Sequence Data
>OriGene sequence for NM_032335.2 CCCGCTCTCAGGCACTGCTGGAGAACCGAGACCGACTTCTTTCTCTTTACCCTCATTGGC
GCTTCTCTCCTGCAGTCCGCCTCTGGGCCCTGCCGCATTTCTTGAGACTTAAAGTGGCAT
TCTAAAGGCAATTTAAAAATCATGTCAAGCTCAGTTGAACAGAAAAAAGGGCCTACAAGA
CAGCGCAAATGTGGCTTTTGTAAGTCAAATAGAGACAAGGAATGTGGACAGTTACTAATA
TCTGAAAACCAGAAGGTGGCAGCGCACCATAAGTGCATGCTCTTTTCATCTGCTTTGGTA
TCATCACACTCTGATAATGAAAGTCTTGGTGGATTTTCTATTGAAGATGTCCAAAAGGAA
ATTAAAAGAGGCACGAAGCTGATGTGTTCTTTGTGCCATTGTCCTGGAGCAACAATTGGT
TGTGATGTGAAAACATGTCACAGGACATACCACTACCACTGTGCATTGCATGATAAAGCT
CAAATACGAGAGAAACCTTCACAAGGAATTTACATGGCCTATTGCCGAAAACACAAGAAA
ACTGCACATAACTCCGAAGCAGCTGATTTAGAAGAAAGTTTTAATGAACATGAACTGGAG
CCCTCATCACCTAAAAGTAAAAAGAAAAGTCGCAAAGGAAGGCCAAGAAAAACTAATTTT
AAAGGGCTGTCAGAAGATACCAGGTCCACATCCTCCCATGGAACAGATGAAATGGAAAGT
AGTTCCTATAGAGATAGGTCTCCACACAGAAGCAGCCCTAGTGACACCAGGCCTAAATGT
GGATTTTGCCATGTAGGGGAGGAAGAAAATGAAGCACGAGGAAAACTGCATATATTTAAT
GCCAAGAAGGCAGCTGCCCATTATAAGTGCATGTTGTTTTCTTCTGGCACAGTCCAGCTC
ACAACAACATCAAGAGCAGAATTTGGAGACTTTGATATTAAAACTGTACTTCAGGAGATT
AAACGAGGAAAAAGAATGGTCTGTAGTTTTTATATTTGTTATGCAACATTACACTTGATT
TGCTGCTTTAAATTTAGAGTACATCCCAAATTTATCCAGTCATCAGAAAATTTAAAGTAG
TTCGTATGTTAAAGCAAAGTATATATTTGACTTATTTGTAATATAATAAAGGATGCTGAT
GTTACGGAAAAAAAAAAAAAAAAAAAAAAAAAAAA
>OriGene 5' read for NM_032335.2 unedited
GACACTTGTATACGACTCCTATAGGGCGGCCGGGAATTCGGCCATTACGGCCGGGGCCCG
CTCTCAGGCACTGCTGGAGAACCGAGACCGACTTCTTTCTCTTTACCCTCATTGGCGCTT
CTCTCCTGCAGTCCGCCTCTGGGCCCTGCCGCATTTCTTGAGACTTAAAGTGGCATTCTA
AAGGCAATTTAAAAATCATGTCAAGCTCAGTTGAACAGAAAAAAGGGCCTACAAGACAGC
GCAAATGTGGCTTTTGTAAGTCAAATAGAGACAAGGAATGTGGACAGTTACTAATATCTG
AAAACCAGAAGGTGGCAGCGCACCATAAGTGCATGCTCTTTTCATCTGCTTTGGTATCAT
CACACTCTGATAATGAAAGTCTTGGTGGATTTTCTATTGAAGATGTCCAAAAGGAAATTA
AAAGAGGCACGAAGCTGATGTGTTCTTTGTGCCATTGTCCTGGAGCAACAATTGGTTGTG
ATGTGAAAACATGTCACAGGACATACCACTACCACTGTGCATTGCATGATAAAGCTCAAA
TACGAGAGAAACCTTCACAAGGAATTTACATGGCCTATTGCCGAAAACACAAGAAAACTG
CACATAACTCCGAAGCAGCTGATTTAGAAGAAAGTTTTAATGAACATGAACTGGAGCCCT
CATCACCTAAAAGTAAAAAGAAAAGTCGCAAAGGAGGGCCAAGAAAAACTAATTTTAAAG
GGCTGTCAGAGGATACCAGGTCCACATCCTCCCATGGAACAGATGAAATGGAAAGTAGTT
CCTATAGAGATAGGTCTCCACACAGAAGCAGCCCTAGTGACACCAGGCCTAAATGGTGGA
TTTTGCCATGTAGGGGAGGAAGAATGAGCACGAGGAAACTGCTTATATTTATGCAGAAGG
CAGCTGCCATTATAAGGTGGCATGTGG
Restriction Sites Please inquire     
ACCN NM_032335
ORF Size 939 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_032335.2, NP_115711.2
RefSeq Size 1236
RefSeq ORF 939
Locus ID 84295
Protein Families Druggable Genome, Transcription Factors
Gene Summary This gene is a member of the plant homeodomain (PHD)-like finger (PHF) family. It encodes a protein with two PHD-type zinc finger domains, indicating a potential role in transcriptional regulation, that localizes to the nucleolus. Mutations affecting the coding region of this gene or the splicing of the transcript have been associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a disorder characterized by cognitive disability, epilepsy, hypogonadism, hypometabolism, obesity, swelling of subcutaneous tissue of the face, narrow palpebral fissures, and large ears. Alternate splicing results in multiple transcript variants, encoding different isoforms. [provided by RefSeq, Jun 2010]
Transcript Variant: This variant (3) uses an alternate termination site, resulting in a distinct C-terminus (isoform 2).

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