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        產(chǎn)品資料

        WRN, Polyclonal Antibody

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        產(chǎn)品名稱: WRN, Polyclonal Antibody
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        簡單介紹

        WRN, Polyclonal Antibody


        WRN, Polyclonal Antibody  的詳細(xì)介紹
        Product Name

        WRN, Polyclonal Antibody

        Popular Item
        Full Product Name

        WRN

        Product Gene Name

        anti-WRN antibody

        [Similar Products]
        Research Use Only
        For Research Use Only. Not for use in diagnostic procedures.
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        OMIM
        phenotype 604611
        3D Structure
        ModBase 3D Structure for Q14191
        Clonality
        Polyclonal
        Host
        Rabbit
        Species Reactivity
        Human
        Species
        Human
        Immunogen
        Recombinant Protein
        Other Notes
        Small volumes of anti-WRN antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
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        Product Categories/Family for anti-WRN antibody
        Polyclonal
        Applications Tested/Suitable for anti-WRN antibody
        Western Blot (WB)

        Western Blot (WB) of anti-WRN antibody
        Western blot analysis of extracts of various cell lines, using WRN antibody at 1:1000 dilution.
        Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (MBS128200) at 1:10000 dilution.
        Lysates/proteins: 25ug per lane.
        Blocking buffer: 3% nonfat dry milk in TBST.
        Detection: ECL Basic Kit.
        Exposure time: 15s.
        anti-WRN antibody Western Blot (WB) (WB) image
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        NCBI/Uniprot data below describe general gene information for WRN. It may not necessarily be applicable to this product.
        NCBI GI #
        322510082
        NCBI GeneID
        7486
        NCBI Accession #
        Q14191.2 [Other Products]
        UniProt Primary Accession #
        Q14191 [Other Products]
        UniProt Secondary Accession #
        A1KYY9[Other Products]
        UniProt Related Accession #
        Q14191[Other Products]
        Molecular Weight
        1432
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        NCBI Official Full Name
        Werner syndrome ATP-dependent helicase
        NCBI Official Synonym Full Names
        Werner syndrome, RecQ helicase-like
        NCBI Official Symbol
        WRN??[Similar Products]
        NCBI Official Synonym Symbols
        RECQ3; RECQL2; RECQL3
        ??[Similar Products]
        NCBI Protein Information
        Werner syndrome ATP-dependent helicase; exonuclease WRN; recQ protein-like 2; DNA helicase, RecQ-like type 3
        UniProt Protein Name
        Werner syndrome ATP-dependent helicase
        UniProt Synonym Protein Names
        DNA helicase, RecQ-like type 3; RecQ3; Exonuclease WRN (EC:3.1.-.-); RecQ protein-like 2
        Protein Family
        Werner syndrome ATP-dependent helicase
        UniProt Gene Name
        WRN??[Similar Products]
        UniProt Synonym Gene Names
        RECQ3; RECQL2; RecQ3??[Similar Products]
        UniProt Entry Name
        WRN_HUMAN
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        NCBI Summary for WRN
        This gene encodes a member of the RecQ subfamily and the DEAH (Asp-Glu-Ala-His) subfamily of DNA and RNA helicases. DNA helicases are involved in many aspects of DNA metabolism, including transcription, replication, recombination, and repair. This protein contains a nuclear localization signal in the C-terminus and shows a predominant nucleolar localization. It possesses an intrinsic 3' to 5' DNA helicase activity, and is also a 3' to 5' exonuclease. Based on interactions between this protein and Ku70/80 heterodimer in DNA end processing, this protein may be involved in the repair of double strand DNA breaks. Defects in this gene are the cause of Werner syndrome, an autosomal recessive disorder characterized by premature aging. [provided by RefSeq, Jul 2008]
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        UniProt Comments for WRN
        WRN: Multifunctional enzyme that has both magnesium and ATP- dependent DNA-helicase activity and 3'->5' exonuclease activity towards double-stranded DNA with a 5'-overhang. Has no nuclease activity towards single-stranded DNA or blunt-ended double- stranded DNA. Binds preferentially to DNA substrates containing alternate secondary structures, such as replication forks and Holliday junctions. May play an important role in the dissociation of joint DNA molecules that can arise as products of homologous recombination, at stalled replication forks or during DNA repair. Alleviates stalling of DNA polymerases at the site of DNA lesions. Important for genomic integrity. Plays a role in the formation of DNA replication focal centers; stably associates with foci elements generating s for RP-A. Monomer, and homooligomer. May exist as homodimer, homotrimer, homotetramer and/or homohexamer. Homotetramer, or homohexamer, when bound to DNA. Interacts via its N-terminal domain with WRNIP1. Interacts with EXO1, PCNA and SUPV3L1. Belongs to the helicase family. RecQ subfamily.

        Protein type: Nucleolus; DNA-binding; DNA repair, damage; Cell cycle regulation; Helicase; EC 3.6.4.12

        Chromosomal Location of Human Ortholog: 8p12

        Cellular Component: nucleoplasm; MutLalpha complex; centrosome; nucleolus

        Molecular Function: G-quadruplex DNA binding; protein homodimerization activity; ATPase activity; magnesium ion binding; 3'-5' DNA helicase activity; bubble DNA binding; helicase activity; four-way junction helicase activity; Y-form DNA binding; ATP-dependent DNA helicase activity; protein binding; DNA helicase activity; ATP-dependent 3'-5' DNA helicase activity; DNA binding; manganese ion binding; exonuclease activity; protein complex binding; 3'-5' exonuclease activity; ATP binding

        Biological Process: nucleolus to nucleoplasm transport; positive regulation of hydrolase activity; multicellular organismal aging; cell aging; cellular response to starvation; replicative cell aging; response to UV-C; DNA duplex unwinding; DNA recombination; replication fork processing; regulation of apoptosis; DNA synthesis during DNA repair; base-excision repair; double-strand break repair; response to oxidative stress; regulation of growth rate; DNA replication; response to DNA damage stimulus; telomere maintenance; DNA metabolic process; aging

        Disease: Werner Syndrome
        Research Articles on WRN
        1. WRN and BLM act epistatically with DNA2 to promote the long-range resection of double strand break ends in human cells.
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        Precautions
        All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
        Disclaimer
        While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

        It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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