TBX5 (NM_000192) Human Untagged Clone

CAT#: SC120046

TBX5 (untagged)-Human T-box 5 (TBX5), transcript variant 1



  "NM_000192" in other vectors (6)

CNY 2,950.00


货期*
现货

规格
    • 10 ug

Cited in 2 publications.

Product images

经常一起买 (4)
Rabbit Polyclonal Anti-TBX5 Antibody
    • 100 ul

CNY 1,999.00
CNY 3,280.00


TurboFectin Transfection Reagent (1 mL in 1 vial)
    • 1 ml in 1 vial

CNY 4,090.00


DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
    • 5 x 200 ul

CNY 1,280.00


Forward sequencing primer VP1.5, Reverse sequencing primer XL39, 100pmoles each
    • 100 pmol

CNY 480.00

Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Synonyms HOS
Vector pCMV6-XL4
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF within SC120046 sequence for NM_000192 edited (data generated by NextGen Sequencing)
ATGGCCGACGCAGACGAGGGCTTTGGCCTGGCGCACACGCCTCTGGAGCCTGACGCAAAA
GACCTGCCCTGCGATTCGAAACCCGAGAGCGCGCTCGGGGCCCCCAGCAAGTCCCCGTCG
TCCCCGCAGGCCGCCTTCACCCAGCAGGGCATGGAGGGAATCAAAGTGTTTCTCCATGAA
AGAGAACTGTGGCTAAAATTCCACGAAGTGGGCACGGAAATGATCATAACCAAGGCTGGA
AGGCGGATGTTTCCCAGTTACAAAGTGAAGGTGACGGGCCTTAATCCCAAAACGAAGTAC
ATTCTTCTCATGGACATTGTACCTGCCGACGATCACAGATACAAATTCGCAGATAATAAA
TGGTCTGTGACGGGCAAAGCTGAGCCCGCCATGCCTGGCCGCCTGTACGTGCACCCAGAC
TCCCCCGCCACCGGGGCGCATTGGATGAGGCAGCTCGTCTCCTTCCAGAAACTCAAGCTC
ACCAACAACCACCTGGACCCATTTGGGCATATTATTCTAAATTCCATGCACAAATACCAG
CCTAGATTACACATCGTGAAAGCGGATGAAAATAATGGATTTGGCTCAAAAAATACAGCG
TTCTGCACTCACGTCTTTCCTGAGACTGCGTTTATAGCAGTGACTTCTTACCAGAACCAC
AAGATCACGCAATTAAAGATTGAGAATAATCCCTTTGCCAAAGGATTTCGGGGCAGTGAT
GACATGGAGCTGCACAGAATGTCAAGAATGCAAAGTAAAGAATATCCCGTGGTCCCCAGG
AGCACCGTGAGGCAAAAAGTGGCCTCCAACCACAGTCCTTTCAGCAGCGAGTCTCGAGCT
CTCTCCACCTCATCCAATTTGGGGTCCCAATACCAGTGTGAGAATGGTGTTTCCGGCCCC
TCCCAGGACCTCCTGCCTCCACCCAACCCATACCCACTGCCCCAGGAGCATAGCCAAATT
TACCATTGTACCAAGAGGAAAGAGGAAGAATGTTCCACCACAGACCATCCCTATAAGAAG
CCCTACATGGAGACATCACCCAGTGAAGAAGATTCCTTCTACCGCTCTAGCTATCCACAG
CAGCAGGGCCTGGGTGCCTCCTACAGGACAGAGTCGGCACAGCGGCAAGCTTGCATGTAT
GCCAGCTCTGCGCCCCCCAGCGAGCCTGTGCCCAGCCTAGAGGACATCAGCTGCAACACG
TGGCCAAGCATGCCTTCCTACAGCAGCTGCACCGTCACCACCGTGCAGCCCATGGACAGG
CTACCCTACCAGCACTTCTCCGCTCACTTCACCTCGGGGCCCCTGGTCCCTCGGCTGGCT
GGCATGGCCAACCATGGCTCCCCACAGCTGGGAGAGGGAATGTTCCAGCACCAGACCTCC
GTGGCCCACCAGCCTGTGGTCAGGCAGTGTGGGCCTCAGACTGGCCTGCAGTCCCCTGGC
ACCCTTCAGCCCCCTGAGTTCCTCTACTCTCATGGCGTGCCAAGGACTCTATCCCCTCAT
CAGTACCACTCTGTGCACGGAGTTGGCATGGTGCCAGAGTGGAGCGACAATAGCTAA

Clone variation with respect to NM_000192.3
648 c=>t
>OriGene 5' read for NM_000192 unedited
CCGACACTCGTCATTTTGTNAATACGNACTTTCTNTNAGGGNNCGGCCGCGNAATTTCGG
CACCAGGATAAACAGTAATATTTAATTTGTCGGAGACCACAAACCAACCTTGAGCTGGGA
GGTACGTGCTCTTCTTGACAGACGTTGGAAGAAGACCTGGCCTAAAGAGGTCTCTTTTGG
TGGTCCTTTTCAAAGTCTTCACCTGAGCCCTGCTCTCCAGCGAGGCGCACTCCTGGCTTT
TGCGCTCCAAAGAAGAGGTGGGATAGTTGGAGAGCAGAACCTTGCGCGGGCACAGGGCCC
TGGGCGCACCATGGCCGACGCAGACGAGGGCTTTGGCCTGGCGCACACGCCTCTGGAGCC
TGACGCAAAAGACCTGCCCTGCGATTCGAAACCCGAGAGCGCGCTCGGGGCCCCCAGCAA
GTCCCCGTCGTCCCCGCAGGCCGCCTTCACCCAGCAGGGCATGGAGGGAATCAAAGTGTT
TCTCCATGAAAGAGAACTGTGGCTAAAATTCCACGAAGTGGGCACGGAAATGATCATAAC
CAAGGCTGGAAGGCGGATGTTTCCCAGTTACAAAGTGAAGGTGACGGGCCTTAATCCCAA
AACGAAGTACATTCTTCTCATGGACATTGTACCTGCCGACGATCACAGATACAAATTCGC
AGATAATAAATGGTCTGTGACGGGCAAAGCTGAGCCCGCCATGCCTGGCCGCCTGTACGT
GCACCCAGACTCCCCCGCCACCGGGGCGCATTGGATGAAGCAGCTCGTCTCCTTCCCAGA
AACTCAGCTCACCACAACCACCTGGACCCTTTGGGCATATTATTCTAAATTCATGCANCA
ATACCAGCCTAGATTACACATCGTGAAAGCGGATGAAAATATGGATTNGNCTCAAAAATA
CACCGTCT
>OriGene 3' read for NM_000192 unedited
GGAAAAAAACAATATATTAACAAAAAAACACAAACTTGGTTTCTGAGTATCAATAAAATT
AAAAGCTCTTGGCCAGCTCCTATGCTGGGTTTCATTTCATGTTATTACTTAATTAGAATT
CCTATTTATAAATAAATAGTACCAGTAAAATATTACATCTGAAGAACCCTACCATAACAC
TTTACTTACACACTTTTTCCAATACTGTTTTCGGCTTTCAGTAAACACAGTTCTGTGTCG
GCATTGGTGTGGGCGTGGTTTCTTTGGCGAGATATCATTGCCGACTGTGCCCTGTCTCTT
CTGTAGGAACCGTGTATTTTGCTTGACATCCACTTTGCCCCGTTTTTCACGGACGTTTGG
AACGCTGGTTCCTGCCCTGTTTCCTCCTAACACATGCCTCTTTTATTAATAACCCCATTT
CGGTTTTTCCGTCTCAACTCTTCCCACACCCTTCTCGCCCCTGCCATTACATTCCTGCCG
CACCGTCCACCGCGTTTCTTTCCTCTCGCCCATTTCCGCCTTTCCCCCCTTTTTTTTCTT
TTCTCCCCCCCCCCCGACAGGCATTTTTTCAGTCTTTCCCGCGCTTTCCGGCGTCGCCCT
TTTTTTCCCCCCTTCTCCTTTTTCCCGTATCGGGCCCCCTCCTTTTCCCGCCGTTTTCCC
CCCGCCATTTTTTGGTTTTTTTTTTTCGCGCCCCCGCGTTGTGCAAAACCCGCTCTCTCC
CCCCCCTTTTTTCTCGTTGTTTTTTTCTCCCCCCTCTTTTTTCTCCTCTTGTTTTTTGTG
TCCACGTTTTCCGAATTGCCCTCGTCACCCGCCGGCTCTGCCGGCCCCTTTTTTTTTTTT
TCGCCCCCTTTTTTCCCCCTCCCCCCCGTCTTTTGT
Restriction Sites NotI-NotI     
ACCN NM_000192
Insert Size 1557 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 ORF clone is ion-exchange column purified and shipped in a 2D barcoded Matrix tube containing 10ug of transfection-ready, dried plasmid DNA (reconstitute with 100 ul of water).
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_000192.3, NP_000183.2
RefSeq Size 3921 bp
RefSeq ORF 1557 bp
Locus ID 6910
UniProt ID Q99593
Domains T-box
Protein Families Druggable Genome, Transcription Factors
Gene Summary This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This gene is closely linked to related family member T-box 3 (ulnar mammary syndrome) on human chromosome 12. The encoded protein may play a role in heart development and specification of limb identity. Mutations in this gene have been associated with Holt-Oram syndrome, a developmental disorder affecting the heart and upper limbs. Several transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]
Transcript Variant: This variant (1) represents the longest transcript and encodes the longer isoform (1). Variants 1 and 4 both encode the same 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.
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

Citations (2)

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