B Raf (BRAF) (NM_004333) Human 3' UTR Clone

CAT#: SC207797

3' UTR clone of v-raf murine sarcoma viral oncogene homolog B1 (BRAF) for miRNA target validation



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CNY 4,845.00


货期*
3周

规格
    • 10 ug

Product images

经常一起买 (2)
Firefly luciferase assay kit, 150 assays
    • 1 kit

CNY 1,520.00


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

CNY 1,280.00

Specifications

Product Data
Product Name B Raf (BRAF) (NM_004333) Human 3' UTR Clone
Vector pMirTarget
Synonyms B-raf; B-RAF1; BRAF1; NS7; RAFB1
ACCN NM_004333
Insert Size 2000 bp
Sequence Data
>SC207797 3’UTR clone of NM_004333
The sequence shown below is from the reference sequence of NM_004333. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
GGGGGATATGGTGCGTTTCCTGTCCACTGAAACAAATGAGTGAGAGAGTTCAGGAGAGTAGCAACAAAA
GGAAAATAAATGAACATATGTTTGCTTATATGTTAAATTGAATAAAATACTCTCTTTTTTTTTAAGGTG
AACCAAAGAACACTTGTGTGGTTAAAGACTAGATATAATTTTTCCCCAAACTAAAATTTATACTTAACA
TTGGATTTTTAACATCCAAGGGTTAAAATACATAGACATTGCTAAAAATTGGCAGAGCCTCTTCTAGAG
GCTTTACTTTCTGTTCCGGGTTTGTATCATTCACTTGGTTATTTTAAGTAGTAAACTTCAGTTTCTCAT
GCAACTTTTGTTGCCAGCTATCACATGTCCACTAGGGACTCCAGAAGAAGACCCTACCTATGCCTGTGT
TTGCAGGTGAGAAGTTGGCAGTCGGTTAGCCTGGGTTAGATAAGGCAAACTGAACAGATCTAATTTAGG
AAGTCAGTAGAATTTAATAATTCTATTATTATTCTTAATAATTTTTCTATAACTATTTCTTTTTATAAC
AATTTGGAAAATGTGGATGTCTTTTATTTCCTTGAAGCAATAAACTAAGTTTCTTTTTATAAATTTTGA
GTGCAGGTGACCAAAAATATTGCTGAGGAGTGGCACGTTTGACATGAGTAAAATGTCTTAACTTCGGAT
TTTTAGCGGGAAAATGTTATAAATTGGAGTTTCTTTTAAATAGCTTTTTTTAAAATACATTAAGGATGT
CTCGCTCATGTAGAAGTCAAATTTTGTTGCAAACGCATTGCTCCCTTCACACCCAATCTCTCCCCTGCA
AAAAATCTTCACAGAATTCTGTGAGAACTTTTAGGTGTGTTTTTCTTTGAGATACCTCTGGTTGCCAAA
CACCAGGTAATAGATTTTTTAAAGTTGTTATTAGATTATTCTTACCTCTCATGATGCATATTTTAGCAA
TCACCTTATCATTGTGTCTCATGTTCTGTCCTCCTTATATTCTTTGCCCAGCAAGATTCTACTTATGAT
GAATGAATGCTCTTCTCCTTTTTTCATTCAATGGTATGAAGTATTTGTTAGGGTTCTTTAGTACTTACA
CTTTGTTGTGTAGAAAATGACTGTAATGTGGTGGTCAGTGTATTCTTACTGTGATTCAGAGGGAATCAA
AAGTAGAAAGCAACAGCACGTGGTCCTATCAAAGATTTGGCCATCTCTGCTTCACTGTCAGCCTCTTAA
CTATATCTTCACTTACTCAATTTGGTTTTGTCATGATTTTTAAATGTAGCCAATAGATCAAGGTTCTTC
CAGTAAACACATATCTGCATAAATGCCTCCTTGAAGTCAATAAAGAAGGAAATTGAGAAGACTTTAAAT
TAATGATAATTTAGTTTTTAAGTACCCACAAATAAATTTTTGAAACATTTTCTTTATTTGAATACTTAG
ATGTCATCCAGGAAAATCACTCAATAATAATTACGGCAAATCTTTAACCCCTCATTTGGGTAGCTTAAG
ATAAGTAATGCCATTATGAATCAGAATTGATTCATGACTTTAGTTAAGAAAATGAAAAGGAACATTTCA
CGTATTTTTAAAAATGATACTAAGGAATAAAGAAGTACAACTATTGGAAAATATCTAAGTATATGATTT
TTAAATCCTCCAGTGGCATTAAATATATGATTATTAGTAATTGTTAGATAGGGTTTTATTCATTCACAA
ATAGAAGACTAGCAAGCATGTAACTAACAAAGTTTTTACAAAATTGACTTTGTGGAATGCTCCAAATGT
TTGGCCATTTTGAGGCACAAGGTCAGGGGTCTCTTTATTGATAGAGCTCCTTCTATAATTTCCCAGCAT
ACCTGCCTCACAGTTATCTTCCTTTCATTGTTCACTCTCTTTTTCTTCTCAATGCCATCCTGCCTAGGC
TCCCATCATCTGCATCTGACACCTTTCCTTTCTTTCTTTACTAGTCTCCTTTGCGATGGGTGTGGCTA
ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA
CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG
Restriction Sites SgfI-MluI     
OTI Disclaimer Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs).
Reference Data
RefSeq NM_004333.6
Synonyms B-raf; B-RAF1; BRAF1; NS7; RAFB1
Summary This gene encodes a protein belonging to the RAF family of serine/threonine protein kinases. This protein plays a role in regulating the MAP kinase/ERK signaling pathway, which affects cell division, differentiation, and secretion. Mutations in this gene, most commonly the V600E mutation, are the most frequently identified cancer-causing mutations in melanoma, and have been identified in various other cancers as well, including non-Hodgkin lymphoma, colorectal cancer, thyroid carcinoma, non-small cell lung carcinoma, hairy cell leukemia and adenocarcinoma of lung. Mutations in this gene are also associated with cardiofaciocutaneous, Noonan, and Costello syndromes, which exhibit overlapping phenotypes. A pseudogene of this gene has been identified on the X chromosome. [provided by RefSeq, Aug 2017]
Locus ID 673
MW 77
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