ZNF195 (NM_007152) Human Untagged Clone
CAT#: SC126999
ZNF195 (untagged)-Human zinc finger protein 195 (ZNF195), transcript variant 3
"NM_007152" in other vectors (2)
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Specifications
Product Data | |
Type | Human Untagged Clone |
Tag | Tag Free |
Symbol | ZNF195 |
Synonyms | HRF1; ZNFP104 |
Vector | pCMV6-XL5 |
E. coli Selection | Ampicillin (100 ug/mL) |
Mammalian Cell Selection | None |
Sequence Data |
>OriGene ORF within SC126999 sequence for NM_007152 edited (data generated by NextGen Sequencing)
ATGACTCTGTTGACGTTCAGGGATGTGGCCATAGAATTCTCCCTGGAGGAGTGGAAATGC CTGGACCTCGCTCAGCAGAATTTGTACAGGGATGTGATGTTGGAGAACTACAGAAACTTG TTCTCCGTTGGTCTCACTGTCTGTAAGCCAGGCCTGATCACCTGCCTGGAGCAACGAAAA GAGCCCTGGAATGTGAAGAGACAGGAGGCAGCAGACGGACATCCAGCTATGTCTTCTCAT TTTACCCAAGACCTTCTGCCAGAGCAGGGCATACAAGATGCATTCCCAAAAAGAATACTG AGAGGATATGGAAATTGTGGCCTTGATAATTTATATTTAAGGAAAGACTGGGAAAGTTTA GATGAGTGTAAGTTGCAAAAAGATTATAATGGACTTAACCAATGTTCATCAACTACCCAT AGCAAAATCTTTCAATATAATAAATATGTTAAAATCTTTGATAACTTTTCAAATTTACAT AGACGTAATATAAGTAATACTGGAGAGAAACCTTTCAAATGTCAAGAATGTGGCAAATCC TTTCAAATGCTCTCATTCCTAACTGAACATCAGAAAATTCACACTGGAAAAAAATTCCAA AAATGTGGAGAATGTGGCAAAACCTTTATCCAGTGCTCACACTTTACTGAACCTGAGAAC ATTGACACTGGAGAGAAACCTTACAAGTGTCAAGAATGTAACAACGTCATTAAAACTTGC TCAGTCCTTACTAAAAATAGAATTTATGCCGGAGGGGAACATTACAGATGTGAAGAATTT GGCAAAGTATTTAACCAGTGCTCCCACCTTACTGAACATGAGCATGGTACTGAGGAAAAA CCCTGCAAATATGAAGAGTGCAGCAGTGTCTTTATCTCTTGCTCAAGCCTTTCTAATCAA CAGATGATTCTTGCTGGAGAGAAGCTCTCCAAATGTGAAACATGGTACAAAGGTTTTAAC CACAGCCCAAATCCTTCCAAACACCAGAGAAATGAGATTGGAGGGAAACCTTTCAAATGT GAGGAATGTGACAGCATCTTCAAGTGGTTCTCAGACCTTACTAAACATAAGAGAATTCAC ACTGGTGAGAAACCATACAAATGTGACGAATGTGGGAAAGCCTATACACAGTCCTCACAC CTCAGTGAACACAGGAGGATTCACACCGGAGAGAAACCCTACCAATGTGAAGAATGTGGG AAGGTCTTCAGAACTTGCTCAAGCCTTTCTAACCATAAGAGAACTCATTCTGAAGAAAAA CCCTACACGTGTGAAGAATGTGGCAACATCTTTAAGCAGTTATCAGACCTCACTAAGCAT AAGAAAACCCATACTGGAGAGAAGCCCTACAAATGTGACGAATGTGGAAAAAACTTTACC CAGTCCTCCAACCTTATTGTACATAAGAGAATTCATACTGGAGAGAAACCCTACAAGTGT GAAGAATGTGGCAGAGTCTTCATGTGGTTCTCAGACATTACCAAACATAAGAAAACCCAT ACTGGAGAGAAACCCTACAAATGTGACGAATGTGGAAAAAACTTTACCCAGTCCTCAAAC CTTATTGTACATAAGAGAATTCATACTGGAGAGAAACCCTACAAGTGTGAAAAGTGTGGC AAAGCCTTCACCCAGTTCTCACACCTGACTGTACATGAAAGCATTCATACTTGA Clone variation with respect to NM_007152.4 >OriGene 5' read for NM_007152 unedited
ATTTTGTAATACGAACTCCTATAGGGCGGCCGCGAATTCGGCACGAGGGTCCCCTGCTAG CCGTAGGCCGTGTGACCCGCAGGCACCGGGAGATCCAGAAGTGAAACGCCAGGCTCTCTG GAGGCCAGGAGATGACTCTGTTGACGTTCAGGGATGTGGCCATAGAATTCTCCCTGGAGG AGTGGAAATGCCTGGACCTCGCTCAGCAGAATTTGTACAGGGATGTGATGTTGGAGAACT ACAGAAACTTGTTCTCCGTTGGTCTCACTGTCTGTAAGCCAGGCCTGATCACCTGCCTGG AGCAACGAAAAGAGCCCTGGAATGTGAAGAGACAGGAGGCAGCAGACGGACATCCAGCTA TGTCTTCTCATTTTACCCAAGACCTTCTGCCAGAGCAGGGCATACAAGATGCATTCCCAA AAAGAATACTGAGAGGATATGGAAATTGTGGCCTTGATAATTTATATTTAAGGAAAGACT GGGAAAGTTTAGATGAGTGTAAGTTGCAAAAAGATTATAATGGACTTAACCAATGTTCAT CAACTACCCATAGCAAAATCTTTCAATATAATAAATATGTTAAAATCTTTGATAACTTTT CAAATTTACATAGACCGTATATAAGTAATACTGGAGAGAAACCTTTCAAATGTCAAGAAT GTGGCANATCCTTTCAAATGCTCTCATTCCTAACTGAACATCAGAAAATTCACACTGGAA AAAAATTCCAAAAATGTGGAGAATGTGGCANAACCTTTATCCAGTGCTCACACTTTACCT GACCTGAGAACATTGACACTGGNAGAGAACCTTACCAGTGTCAAGAATGGTACAACGTCA TTAAAACTTGCTCAGTCCTTACTAAAATAGAANTTATGCCCGAG >OriGene 3' read for NM_007152 unedited
GACCGCGGCCGCAATCTAGAGTCGAGTTTTTTTTTTTTTTTTTTCTCTCTACCAAAATTT TACTCACGCATCTTACATTTCAGTGTCTTTCACCTTTCACGGACAAGTATATCAGTGATG CACACCTAAGAGAAAAGAATTTCTCATATCTCTGACGCAGCAACAACTGACCATGTGTTT TCACATCAGCACTAGAAATGAAGACACAGCATCTACTGATTTGAGAATAGAATGACATCA ATATTCGCTTTTCAAAAATTTAACATTTTTTCAATGCAAAAAAGTATATTTTGAATGTAA TTATAACTCTACAAAAACTCAGTCTCATCCTCCTTTTAAACTTAAATATAAATGATCTAT TTTAAGTCTAGATGTCTCTGTAGACTCAACACAGGGATTCAGTGTCATTTCTGAACGTGT CCGTGCTCTATTCCTTTCTCCTTCAAATCCTCCATTGTTTACTTAAATTGGATTTTGCTT ATTTTTCCATTTAGTGTATTTGCAAAATATCTTTTAGTATGAACTCTAGTGTTTTCTAAG CTATCATTTTTGAACAAATGTTATTCCACATTTATGAGATTTGTTGGGTTTCTCTACAAA TTTTCTGAAAGTTTAAGCAACTGATGCAAGTCTTCCATCTAGTATAATTGTAACATTTTT TTCAGAAGAAATACTCTTGTGTGCTCTGGAGACTTATATTTCATGAAAGGTCTTTCAATA GTAATTACATTTATGATAACTTTATTAAGTCTGAACTCTGATGTAAAGTGGGGATGCGAG CAGATACTAACGGCCTTGCCCTATTTTATATTGGTTATTTCTTTCTCAGTATGAATGCTT TCATTACAGTCAGGTGTGAGACTGGGTGAGGCTTTGCCCACTTTTACACTTGTAGGTTCT CTCCATATGAATCTCTTAGACATAAGGTTGG |
Restriction Sites | NotI-NotI |
ACCN | NM_007152 |
Insert Size | 2560 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). |
Product Components | The cDNA clone is shipped in a 2-D bar-coded Matrix tube as dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials. Every lot of primer is tested to provide clean sequencing of OriGene TrueClones. |
Reconstitution | 1. Centrifuge at 5,000xg for 5min. 2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA. 3. Close the tube and incubate for 10 minutes at room temperature. 4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom. 5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C. |
Reference Data | |
RefSeq | NM_007152.1, NP_009083.1 |
RefSeq Size | 2394 bp |
RefSeq ORF | 1890 bp |
Locus ID | 7748 |
Cytogenetics | 11p15.4 |
Domains | KRAB, zf-C2H2 |
Protein Families | Transcription Factors |
Gene Summary | 'This gene encodes a protein belonging to the Krueppel C2H2-type zinc-finger protein family. These family members are transcription factors that are implicated in a variety of cellular processes. This gene is located near the centromeric border of chromosome 11p15.5, next to an imprinted domain that is associated with maternal-specific loss of heterozygosity in Wilms' tumors. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]' Transcript Variant: This variant (3) lacks two alternate in-frame exons in the 3' coding region, compared to variant 1, resulting in an isoform (3) that is shorter than 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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