Frizzled 9 (FZD9) (NM_003508) Human Untagged Clone

CAT#: SC117912

FZD9 (untagged)-Human frizzled family receptor 9 (FZD9)



  "NM_003508" 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-FZD9 antibody
    • 100 ul

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 CD349; FZD3
Vector pCMV6-XL4
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF within SC117912 sequence for NM_003508 edited (data generated by NextGen Sequencing)
ATGGCCGTAGCGCCTCTGCGGGGGGCGCTGCTGCTGTGGCAGCTGCTGGCGGCGGGCGGC
GCGGCACTGGAGATCGGCCGCTTCGACCCGGAGCGCGGGCGCGGGGCTGCGCCGTGCCAG
GCGGTGGAGATCCCCATGTGCCGCGGCATCGGCTACAACCTGACCCGCATGCCCAACCTG
CTGGGCCACACGTCGCAGGGCGAGGCGGCTGCCGAGCTAGCGGAGTTCGCGCCGCTGGTG
CAGTACGGCTGCCACAGCCACCTGCGCTTCTTCCTGTGCTCGCTCTACGCGCCCATGTGC
ACCGACCAGGTCTCGACGCCCATTCCCGCCTGCCGGCCCATGTGCGAGCAGGCGCGCCTG
CGCTGCGCGCCCATCATGGAGCAGTTCAACTTCGGCTGGCCGGACTCGCTCGACTGCGCC
CGGCTGCCCACGCGCAACGACCCGCACGCGCTGTGCATGGAGGCGCCCGAGAACGCCACG
GCCGGCCCCGCGGAGCCCCACAAGGGCCTGGGCATGCTGCCCGTGGCGCCGCGGCCCGCG
CGCCCTCCCGGAGACCTGGGCCCGGGCGCGGGCGGCAGTGGCACCTGCGAGAACCCCGAG
AAGTTCCAGTACGTGGAGAAGAGCCGCTCGTGCGCACCGCGCTGCGGGCCCGGCGTCGAG
GTGTTCTGGTCCCGGCGCGACAAGGACTTCGCGCTGGTCTGGATGGCCGTGTGGTCGGCG
CTGTGCTTCTTCTCCACCGCCTTCACTGTGCTCACCTTCTTGCTGGAGCCCCACCGCTTC
CAGTACCCCGAGCGCCCCATCATCTTCCTCTCCATGTGCTACAACGTCTACTCGCTGGCC
TTCCTGATCCGTGCGGTGGCCGGAGCGCAGAGCGTGGCCTGTGACCAGGAGGCGGGCGCG
CTCTACGTGATCCAGGAGGGCCTGGAGAACACGGGCTGCACGCTGGTCTTCCTACTGCTC
TACTACTTCGGCATGGCCAGCTCGCTCTGGTGGGTGGTCCTGACGCTCACCTGGTTCCTG
GCTGCCGGGAAGAAATGGGGCCACGAGGCCATCGAGGCCCACGGCAGCTATTTCCACATG
GCTGCCTGGGGCCTGCCCGCGCTCAAGACCATCGTCATCCTGACCCTGCGCAAGGTGGCG
GGTGATGAGCTGACTGGGCTTTGCTACGTGGCCAGCACGGATGCAGCAGCGCTCACGGGC
TTCGTGCTGGTGCCCCTCTCTGGCTACCTGGTGCTGGGCAGTAGTTTCCTCCTGACCGGC
TTCGTGGCCCTCTTCCACATCCGCAAGATCATGAAGACGGGCGGCACCAACACAGAGAAG
CTGGAGAAGCTCATGGTCAAGATCGGGGTCTTCTCCATCCTCTACACGGTGCCCGCCACC
TGCGTCATCGTTTGCTATGTCTACGAACGCCTCAACATGGACTTCTGGCGCCTTCGGGCC
ACAGAGCAGCCATGCGCAGCGGCCGCGGGGCCCGGAGGCCGGAGGGACTGCTCGCTGCCA
GGGGGCTCGGTGCCCACCGTGGCGGTCTTCATGCTCAAAATTTTCATGTCACTGGTGGTG
GGGATCACCAGCGGCGTCTGGGTGTGGAGCTCCAAGACTTTCCAGACCTGGCAGAGCCTG
TGCTACCGCAAGATAGCAGCTGGCCGGGCCCGGGCCAAGGCCTGCCGCGCCCCCGGGAGC
TACGGACGTGGCACGCACTGCCACTATAAGGCTCCCACCGTGGTCTTGCACATGACTAAG
ACGGACCCCTCTTTGGAGAACCCCACACACCTCTAG

Clone variation with respect to NM_003508.2
9 g=>a
>OriGene 5' read for NM_003508 unedited
CGCNAACTTTGGTTTNAATANACNANATTCAGGAGAGGGNCGGAACGCCAGTGTGTTGGG
TATCTGCAGATTTCGGCTTGGGCCTCCCGGGATGGCCGTAGCGCCTCTGCGGGGGGCGCT
GCTGCTGTGGCAGCTGCTGGCGGCGGGCGGCGCGGCACTGGAGATCGGCCGCTTCGACCC
GGAGCGCGGGCGCGGGGCTGCGCCGTGCCAGGCGGTGGAGATCCCCATGTGCCGCGGCAT
CGGCTACAACCTGACCCGCATGCCCAACCTGCTGGGCCACACGTCGCAGGGCGAGGCGGC
TGCCGAGCTAGCGGAGTTCGCGCCGCTGGTGCAGTACGGCTGCCACAGCCACCTGCGCTT
CTTCCTGTGCTCGCTCTACGCGCCCATGTGCACCGACCAGGTCTCGACGCCCATTCCCGC
CTGCCGGCCCATGTGCGAGCAGGCGCGCCTGCGCTGCGCGCCCATCATGGAGCAGTTCAA
CTTCGGCTGGCCGGACTCGCTCGACTGCGCCCGGCTGCCCACGCGCAACGACCCGCACGC
GCTGTGCATGGAGGCGCCCGAGAACGCCACGGCCGGCCCCGCGGAGCCCCACAAGGGCCT
GGGCATGCTGCCCGTGGCGCCGCGGCCCGCGCGCCCTCCCGGAGACCTGGGCCCGGGCGC
GGGCGGCAGTGGCACCTGCGAGAACCCCGAGAAGTTCCAGTACGTGGAGAAGAGCCGCTC
GTGCGCACCGCGCTGCGGGCCCGGCGTCGAGGTGTTCTGGTCCCGGCGCGACAAGGACTT
CGCGCTGGTCTGGATGGCCGTGTGGTCGGCGCTGTGCTTCTTCTNCACCGNCTTCACTGT
GCTCACCTTNCTTGCTGGAGCCCCACCGCTTNCAGTACCCCGAGCGCCCCATCAT
>OriGene 3' read for NM_003508 unedited
GATCGACAAACTTGCTATCGGTACCGAGCTCGGATCCACTAGTAACGGCCGCCAGTGTGC
TGGAATTCGGCTTTGTGTGGCTAGAGGTGTGTGGGGTTCTCCAAAGAGGGGTCCGTCTTA
GTCATGTGCAAGACCACGGTGGGAGCCTTATAGTGGCAGTGCGTGCCACGTCCGTAGCTC
CCGGGGGCGCGGCAGGCCTTGGCCCGGGCCCGGCCAGCTGCTATCTTGCGGTAGCACAGG
CTCTGCCAGGTCTGGAAAGTCTTGGAGCTCCACACCCAGACGCCGCTGGTGATCCCCACC
ACCAGTGACATGAAAATTTTGAGCATGAAGACCGCCACGGTGGGCACCGAGCCCCCTGGC
AGCGAGCAGTCCCTCCGGCCTCCGGGCCCGCGGCCGCTGCGCATGGCTGCTCTGTGGCCC
GAAGGCGCCAGAAGTCCATGTTGAGGCGTTCGTAGACATAGCAAACGATGACGCAGGTGG
CGGGCACCGTGTAGAGGATGGAGAAGACCCCGATCTTGACCATGAGCTTCTCCAGCTTCT
CTGTGTTGGTGCCGCCCGTCTTCATGATCTTGCGGATGTGGAAGAGGGCCACGAAGCCGG
TCAGGAGGAAACTACTGCCCAGCACCAGGTAGCCAGAGAGGGGCACCAGCACGAAGCCCG
TGAGCGCTGCTGCATCCGTGCTGGCCACGTAGCAAAGCCCAGTCAGCTCATCACCCGCCA
CCTTGCGCAGGGTCAGGATGACGATGGTCTTGAGCGCGGGCAGGCCCCAGGCAGCCATGT
GGAAATAGCTGCCGTGGGCCTCGATGGCCTCGTGCCCCATTTCTTCCCGCAGCCAGGAAC
CAGTGAGCGTCAGGACCACCCACCAGAGCGAGCT
Restriction Sites Please inquire     
ACCN NM_003508
Insert Size 2000 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_003508.2, NP_003499.1
RefSeq Size 2342 bp
RefSeq ORF 1776 bp
Locus ID 8326
UniProt ID O00144
Protein Families Druggable Genome, GPCR, Transmembrane
Protein Pathways Basal cell carcinoma, Colorectal cancer, Melanogenesis, Pathways in cancer, Wnt signaling pathway
Gene Summary Members of the 'frizzled' gene family encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD9 gene is located within the Williams syndrome common deletion region of chromosome 7, and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype. FZD9 is expressed predominantly in brain, testis, eye, skeletal muscle, and kidney. [provided by RefSeq, Jul 2008]
*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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