RUNX2 (NM_004348) Human Untagged Clone

CAT#: SC123971

RUNX2 (untagged)-Human runt-related transcription factor 2 (RUNX2), transcript variant 3



  "NM_004348" in other vectors (6)

CNY 3,784.00

CNY 8,080.00


货期*
现货

规格
    • 10 ug

Cited in 1 publication.

Product images

经常一起买 (4)
RUNX2 mouse monoclonal antibody, clone OTI3E12
    • 100 ul

CNY 1,999.00
CNY 3,600.00


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 AML3; CBFA1; CCD; CCD1; OSF-2; OSF2; PEA2aA; PEBP2A1; PEBP2A2; PEBP2aA; PEBP2aA1
Vector pCMV6-XL4
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF within SC123971 sequence for NM_004348 edited (data generated by NextGen Sequencing)
ATGCGTATTCCCGTAGATCCGAGCACCAGCCGGCGCTTCAGCCCCCCCTCCAGCAGCCTG
CAGCCCGGCAAAATGAGCGACGTGAGCCCGGTGGTGGCTGCGCAACAGCAGCAGCAACAG
CAGCAGCAGCAACAGCAGCAGCAGCAGCAGCAACAGCAGCAGCAGCAGCAGGAGGCGGCG
GCGGCGGCTGCGGCGGCGGCGGCGGCTGCGGCGGCGGCAGCTGCAGTGCCCCGGTTGCGG
CCGCCCCACGACAACCGCACCATGGTGGAGATCATCGCCGACCACCCGGCCGAACTCGTC
CGCACCGACAGCCCCAACTTCCTGTGCTCGGTGCTGCCCTCGCACTGGCGCTGCAACAAG
ACCCTGCCCGTGGCCTTCAAGGTGGTAGCCCTCGGAGAGGTACCAGATGGGACTGTGGTT
ACTGTCATGGCGGGTAACGATGAAAATTATTCTGCTGAGCTCCGGAATGCCTCTGCTGTT
ATGAAAAACCAAGTAGCAAGGTTCAACGATCTGAGATTTGTGGGCCGGAGTGGACGAGGC
AAGAGTTTCACCTTGACCATAACCGTCTTCACAAATCCTCCCCAAGTAGCTACCTATCAC
AGAGCAATTAAAGTTACAGTAGATGGACCTCGGGAACCCAGAAGGCACAGACAGAAGCTT
GATGACTCTAAACCTAGTTTGTTCTCTGACCGCCTCAGTGATTTAGGGCGCATTCCTCAT
CCCAGTATGAGAGTAGGTGTCCCGCCTCAGAACCCACGGCCCTCCCTGAACTCTGCACCA
AGTCCTTTTAATCCACAAGGACAGAGTCAGATTACAGACCCCAGGCAGGCACAGTCTTCC
CCGCCGTGGTCCTATGACCAGTCTTACCCCTCCTACCTGAGCCAGATGACGTCCCCGTCC
ATCCACTCTACCACCCCGCTGTCTTCCACACGGGGCACTGGGCTTCCTGCCATCACCGAT
GTGCCTAGGCGCATTTCAGATGATGACACTGCCACCTCTGACTTCTGCCTCTGGCCTTCC
ACTCTCAGTAAGAAGAGCCAGGCAGGTGCTTCAGAACTGGGCCCTTTTTCAGACCCCAGG
CAGTTCCCAAGCATTTCATCCCTCACTGAGAGCCGCTTCTCCAACCCACGAATGCACTAT
CCAGCCACCTTTACTTACACCCCGCCAGTCACCTCAGGCATGTCCCTCGGTATGTCCGCC
ACCACTCACTACCACACCTACCTGCCACCACCCTACCCCGGCTCTTCCCAAAGCCAGAGT
GGACCCTTCCAGACCAGCAGCACTCCATATCTCTACTATGGCACTTCGTCAGGATCCTAT
CAGTTTCCCATGGTGCCGGGGGGAGACCGGTCTCCTTCCAGAATGCTTCCGCCATGCACC
ACCACCTCGAATGGCAGCACGCTATTAAATCCAAATTTGCCTAACCAGAATGATGGTGTT
GACGCTGATGGAAGCCACAGCAGTTCCCCAACTGTTTTGAATTCTAGTGGCAGAATGGAT
GAATCTGTTTGGCGACCATATTGA

Clone variation with respect to NM_004348.3
>OriGene 5' read for NM_004348 unedited
ACTGCAGTGCACTTNCGAGAGNATATGGCGAACGCGAACTGGGGGCCAGGTCTCGCCTTC
ACCCCCCCAATTTCCTCCTTGCCCTTTATTTCCACCCTCCTCCCCCTCCCCCGGCGGGTT
CGCTAACTTGTGGCTGTGGGTGATGCGTATTCCCGTAGATCCGAGCACCAGCCGGCGCTT
CAGCCCCCCCTCCAGCAGCCTGCAGCCCGGCAAAATGAGCGACGTGAGCCCGGTGGTGGC
TGCGCAACAGCAGCAGCAACAGCAGCAGCAGCAACAGCAGCAGCAGCAGCAGCAACAGCA
GCAGCAGCAGCAGGAGGCGGCGGCGGCGGCTGCGGCGGCGGCGGCGGCTGCGGCGGCGGC
AGCTGCAGTGCCCCGGTTGCGGCCGCCCCACGACAACCGCACCATGGTGGAGATCATCGC
CGACCACCCGGCCGAACTCGTCCGCACCGACAGCCCCAACTTCCTGTGCTCGGTGCTGCC
CTCGCACTGGCGCTGCAACAAGACCCTGCCCGTGGCCTTCAAGGTGGTAGCCCTCGGAGA
GGTACCAGATGGGACTGTGGTTACTGTCATGGCGGGTAACGATGAAAATTATTCTGCTGA
GCTCCGGAATGCCTCTGCTGTTATGAAAAACCAAGTAGCAAGGTTCAACGATCTGAGATT
TGTGGGCCGGAGTGGACGAGGCAAGAGTTTCACCTTGACCATAACCGTCTTCACAATCCT
CCCCAGTAGCTACCTAT
>OriGene 3' read for NM_004348 unedited
GTATTCTTTGTACCCGCCTGACAGTTACCACAGTCCCATCTGGTAGCTCTCCGAGGGCTA
CCACCTTGAAGGCCACGGGCAGGGTTTTGTTGCAGCGCCAGTGCGAGGGCAGCACCGAGC
ACAGGAAGTTGGGGCTGTCGGTGCGGACGAGTTCGGCCGGGTGGTCGGCGATGATCTCCA
CCATGGTGCGGTTGTCGTGGGGCGGCCGCAACCGGGGCACTGCAGCTGCCGCCGCCGCAG
CCGCCGCCGCCGCCGCAGCCGCCGCCGCCGCCTCCTGCTGCTGCTGCTGCTGTTGCTGCT
GCTGCTGCTGCTGTTGCTGCTGCTGCTGTTGCTGCTGCTGTTGCGCAGCCACCACCGGGC
TCACGTCGCTCATTTTGCCGGGCTGCAGGCTGCTGGAGGGGGGGCTGAAGCGCCGGCTGG
TGCTCGGATCTACGGGAATACGCATCACAACAGCCACAAGTTAGCGAAGTGGCCGGGGGA
GGGGGAGGAGGGTGGAAATGAGGGGCAAGGAGGAAATTGGGGGGGTGAANGCNANNACNN
GNTGCNGAANGNNNGANNNGCCCNAGAGTGAATCGAGATTACAAGAATTTTGGACAGGAT
TTACTAAATGCGACGCTTCGCTTATAGAACAAGTAGCCTACAACACCATGTCTCGACTGG
CATATCGGTGACCATTTTTCACGTCCTCTACCGCGGGCCCTGGTGTATTAATCTGAACGA
GACTGTGTTATGGGAGAGAGGACGACCTCGCCTTGACGTTGTCGAAGACGCGCCGCAGAT
GCCAATATGAGGTCACTGATGTTGGAATCGTCGAGTAATTGGGACGATTGCAGACAGCT
Restriction Sites NotI-NotI     
ACCN NM_004348
Insert Size 5000 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.
Note Plasmids are not sterile.  For experiments where strict sterility is required, filtration with 0.22um filter is required.
Reference Data
RefSeq NM_004348.3, NP_004339.3
RefSeq Size 5720 bp
RefSeq ORF 1524 bp
Locus ID 860
Domains Runt
Protein Families Druggable Genome, Transcription Factors
Gene Summary This gene is a member of the RUNX family of transcription factors and encodes a nuclear protein with an Runt DNA-binding domain. This protein is essential for osteoblastic differentiation and skeletal morphogenesis and acts as a scaffold for nucleic acids and regulatory factors involved in skeletal gene expression. The protein can bind DNA both as a monomer or, with more affinity, as a subunit of a heterodimeric complex. Two regions of potential trinucleotide repeat expansions are present in the N-terminal region of the encoded protein, and these and other mutations in this gene have been associated with the bone development disorder cleidocranial dysplasia (CCD). Transcript variants that encode different protein isoforms result from the use of alternate promoters as well as alternate splicing. [provided by RefSeq, Jul 2016]
Transcript Variant: This variant (3) is transcribed from an alternate promoter (P2) and contains a different segment for the 5' UTR and 5' coding region than variant 1. It encodes a protein (isoform c) with a shorter and distinct N-terminus when it is compared to isoform a.
*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 (1)

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