FANCC (NM_000136) Human Untagged Clone

CAT#: SC120069

FANCC (untagged)-Human Fanconi anemia, complementation group C (FANCC)


  "NM_000136" in other vectors (6)

Reconstitution Protocol

USD 310.00

In Stock*

Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol FANCC
Synonyms FA3; FAC; FACC
Vector pCMV6-XL5
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF within SC120069 sequence for NM_000136 edited (data generated by NextGen Sequencing)
ATGGCTCAAGATTCAGTAGATCTTTCTTGTGATTATCAGTTTTGGATGCAGAAGCTTTCT
GTATGGGATCAGGCTTCCACTTTGGAAACCCAGCAAGACACCTGTCTTCACGTGGCTCAG
TTCCAGGAGTTCCTAAGGAAGATGTATGAAGCCTTGAAAGAGATGGATTCTAATACAGTC
ATTGAAAGATTCCCCACAATTGGTCAACTGTTGGCAAAAGCTTGTTGGAATCCTTTTATT
TTAGCATATGATGAAAGCCAAAAAATTCTAATATGGTGCTTATGTTGTCTAATTAACAAA
GAACCACAGAATTCTGGACAATCAAAACTTAACTCCTGGATACAGGGTGTATTATCTCAT
ATACTTTCAGCACTCAGATTTGATAAAGAAGTTGCTCTTTTCACTCAAGGTCTTGGGTAT
GCACCTATAGATTACTATCCTGGTTTGCTTAAAAATATGGTTTTATCATTAGCGTCTGAA
CTCAGAGAGAATCATCTTAATGGATTTAACACTCAAAGGCGAATGGCTCCCGAGCGAGTG
GCGTCCCTGTCACGAGTTTGTGTCCCACTTATTACCCTGACAGATGTTGACCCCCTGGTG
GAGGCTCTCCTCATCTGTCATGGACGTGAACCTCAGGAAATCCTCCAGCCAGAGTTCTTT
GAGGCTGTAAACGAGGCCATTTTGCTGAAGAAGATTTCTCTCCCCATGTCAGCTGTAGTC
TGCCTCTGGCTTCGGCACCTTCCCAGCCTTGAAAAAGCAATGCTGCATCTTTTTGAAAAG
CTAATCTCCAGTGAGAGAAATTGTCTGAGAAGGATCGAATGCTTTATAAAAGATTCATCG
CTGCCTCAAGCAGCCTGCCACCCTGCCATATTCCGGGTTGTTGATGAGATGTTCAGGTGT
GCACTCCTGGAAACCGATGGGGCCCTGGAAATCATAGCCACTATTCAGGTGTTTACGCAG
TGCTTTGTAGAAGCTCTGGAGAAAGCAAGCAAGCAGCTGCGGTTTGCACTCAAGACCTAC
TTTCCTTACACTTCTCCATCTCTTGCCATGGTGCTGCTGCAAGACCCTCAAGATATCCCT
CGGGGACACTGGCTCCAGACACTGAAGCATATTTCTGAACTGCTCAGAGAAGCAGTTGAA
GACCAGACTCATGGGTCCTGCGGAGGTCCCTTTGAGAGCTGGTTCCTGTTCATTCACTTC
GGAGGATGGGCTGAGATGGTGGCAGAGCAATTACTGATGTCGGCAGCCGAACCCCCCACG
GCCCTGCTGTGGCTCTTGGCCTTCTACTACGGCCCCCGTGATGGGAGGCAGCAGAGAGCA
CAGACTATGGTCCAGGTGAAGGCCGTGCTGGGCCACCTCCTGGCAATGTCCAGAAGCAGC
AGCCTCTCAGCCCAGGACCTGCAGACGGTAGCAGGACAGGGCACAGACACAGACCTCAGA
GCTCCTGCACAACAGCTGATCAGGCACCTTCTCCTCAACTTCCTGCTCTGGGCTCCTGGA
GGCCACACGATCGCCTGGGATGTCATCACCCTGATGGCTCACACTGCTGAGATAACTCAC
GAGATCATTGGCTTTCTTGACCAGACCTTGTACAGATGGAATCGTCTTGGCATTGAAAGC
CCTAGATCAGAAAAACTGGCCCGAGAGCTCCTTAAAGAGCTGCGAACTCAAGTCTAG

Clone variation with respect to NM_000136.2
>OriGene 5' read for NM_000136 unedited
TTCCTTCAGTCCTGGAAGGCTGCTGTGAAGGAATCACCTTTTCGCTTTTTCCAAGATGGC
TCAAGATTCAGTAGAACTTTCTTGTGATTATCAGTTTTGGATGCAGAAGCTTTCTGTATT
GGGATCAGGCTTCCACTTTGGAAACCCAGCAAGACACCTGTCTTCACGTGGCTCAGTTCC
AGGAGTTCCTAAGGAAGATGTATGAAGCCTTGAAAGAGATGGATTCTAATACAGTCATTG
AAAGATTCCCCACAATTGGTCAACTGTTGGCAAAAGCTTGTTGGAATCCTTTTATTTTAG
CATATGATGAAAGCCAAAAAATTCTAATATGGTGCTTATGTTGTCTAATTAACAAAGAAC
CACAGAATTCTGGACAATCAAAACTTAACTCCTGGATACAGGGTGTATTATCTCATATAC
TTTCAGCACTCAGATTTGATAAAGAAGTTGCTCTTTTCACTCAAGGTCTTGGGTATGCAC
CTATAGATTACTATCCTGGTTTGCTTAAAAATATGGTTTTATCATTAGCGTCTGAACTCA
GAGAGAATCATCTTAATGGATTTAACACTCAAAGGCGAATGGCTCCCGAGCGAGTGGCGT
CCCTGTCACGAGTTTGTGTCCCACTTATTACCCTGACAGATGTTGACCCCCTGGTGGAGG
CTCTCCTCATCTGTCATGGACGTGAACCTCANGAAATCCTCCAGCCAGAGTTCTTTGAGG
CTGTAAACGAGGCCATTTTGCTGAAGAAATTTCTCTCCCCATGTCAGCTGTAGTCTGCCT
CTGGCTTCGGCACCTTCCCAGCCTTGAAAAAGCATGCTGCATCTTTTTGAAAGCTAATCT
CCAGTGAGAGAAATTGTCTGAGT
>OriGene 3' read for NM_000136 unedited
TGAACCGCGGGCCGCAATCTAGNATCGAGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
TTTTTTTTTTTTTTTTTTTTTTTAAAAAAAATAGGGTATTGCCATGTTAACCAGGCAGTC
TGGAACTCCTGGGCTGAAGTAATCCCCCTGCCTTGGCCTCCCAAAGGGCTGGGATCACAG
GGGGGAGCCACTGGACCCAGCCAGGCCAATTTTTTATCAGGAATTTCCAATTCCCATTTC
CATTTAACAAGAAAACTAACTAACTGAATTAATCCTGCCTTTTAATGGTTTTGGAACACA
TTCTTTACCTTCGCCTGGCGGGTTCTTTGATGTCCCAAGGGCCTTTTGGTAGCAGTTAGC
ATCATTTAACAAATACAAAGTGGAAAAAGTGTGCCGGAGGCCCGGGCTTGGGGGGGCTGT
CTGCTCCTGGGGCCCGGCAGGCAGGTCCAGGGAAACACAAGGGAAGCCTGAGGGACCCTG
ACTCCCCTTGAAAAATTTCTCCATACAGCAAGACAGGGGGGCTTTATCCCAAATCCCTGA
CTCCTAAAAAAAGTCTAAAAAGAGCTAAGTTCTCTCTAAATTCTTTAATGGGTCATGACC
AAATTCTTGGTTCTAAGACTTTGAATTTTTAAATAATAGATGTGCAGCTTGACTTGGGTA
AAAACTAAAAACCTGTTCTCCCACCCAAGCCTTTGCTTTAATAATTATTAAACTGACCGT
CTTGCCCGGCGGGCCCCAAAAGACCCCAAGCTCCCTTGAGTATTAAGGAACATGTCTGCC
TGAGTCTGGGCCTGAGGACCCGGCTTCTCCTTTTTGAAAAAAGAAACCAGCAAAATGGCC
CAAGAGGTTTCAGTTTATTTTTACAGCCCAGGAGGGCCTTATCCCAAAAAGGCGGGCCCC
AGGGAATACCGTGCTTGGGCCTGGAG
Restriction Sites NotI-NotI     
ACCN NM_000136
Insert Size 2710 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_000136.2, NP_000127.2
RefSeq Size 4612 bp
RefSeq ORF 1677 bp
Locus ID 2176
Cytogenetics 9q22.32
Domains Fanconi
Protein Families Druggable Genome
Gene Summary 'The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group C. [provided by RefSeq, Jul 2008]'
Transcript Variant: This variant (1) represents the longest transcript and encodes the longer isoform (a).

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