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Recombinant Human TBC domain-containing protein kinase-like protein (TBCK), partial

  • 中文名稱(chēng):
    人TBCK重組蛋白
  • 貨號(hào):
    CSB-YP840579HU
  • 規(guī)格:
  • 來(lái)源:
    Yeast
  • 其他:
  • 中文名稱(chēng):
    人TBCK重組蛋白
  • 貨號(hào):
    CSB-EP840579HU
  • 規(guī)格:
  • 來(lái)源:
    E.coli
  • 其他:
  • 中文名稱(chēng):
    人TBCK重組蛋白
  • 貨號(hào):
    CSB-EP840579HU-B
  • 規(guī)格:
  • 來(lái)源:
    E.coli
  • 共軛:
    Avi-tag Biotinylated

    E. coli biotin ligase (BirA) is highly specific in covalently attaching biotin to the 15 amino acid AviTag peptide. This recombinant protein was biotinylated in vivo by AviTag-BirA technology, which method is BriA catalyzes amide linkage between the biotin and the specific lysine of the AviTag.

  • 其他:
  • 中文名稱(chēng):
    人TBCK重組蛋白
  • 貨號(hào):
    CSB-BP840579HU
  • 規(guī)格:
  • 來(lái)源:
    Baculovirus
  • 其他:
  • 中文名稱(chēng):
    人TBCK重組蛋白
  • 貨號(hào):
    CSB-MP840579HU
  • 規(guī)格:
  • 來(lái)源:
    Mammalian cell
  • 其他:

產(chǎn)品詳情

  • 純度:
    >85% (SDS-PAGE)
  • 基因名:
    TBCK
  • Uniprot No.:
  • 別名:
    Hypothetical protein MGC16169; IHPRF3; MGC16169; TBC domain containing protein kinase like; TBC domain containing protein kinase like protein; TBC domain-containing protein kinase-like protein; TBC1 domain containing kinase; TBCK; TBCK_HUMAN; TBCKL
  • 種屬:
    Homo sapiens (Human)
  • 蛋白長(zhǎng)度:
    Partial
  • 蛋白標(biāo)簽:
    Tag?type?will?be?determined?during?the?manufacturing?process.
    The tag type will be determined during production process. If you have specified tag type, please tell us and we will develop the specified tag preferentially.
  • 產(chǎn)品提供形式:
    Lyophilized powder
    Note: We will preferentially ship the format that we have in stock, however, if you have any special requirement for the format, please remark your requirement when placing the order, we will prepare according to your demand.
  • 復(fù)溶:
    We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference.
  • 儲(chǔ)存條件:
    Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
  • 保質(zhì)期:
    The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself.
    Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.
  • 貨期:
    Delivery time may differ from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
    Note: All of our proteins are default shipped with normal blue ice packs, if you request to ship with dry ice, please communicate with us in advance and extra fees will be charged.
  • 注意事項(xiàng):
    Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week.
  • Datasheet :
    Please contact us to get it.

產(chǎn)品評(píng)價(jià)

靶點(diǎn)詳情

  • 功能:
    Involved in the modulation of mTOR signaling and expression of mTOR complex components. Involved in the regulation of cell proliferation and growth. Involved in the control of actin-cytoskeleton organization.
  • 基因功能參考文獻(xiàn):
    1. We conclude that the c.1854delT variant in the TBCK gene is the mutation causing the congenital brain abnormality in an Arab-Moslem family from northern Israel. PMID: 27748029
    2. RNAsequencing showed that the t(4;5)(q24;q31) resulted in recombination of the genes TBCK on 4q24 and P4HA2 on 5q31.1 with generation of an inframe TBCKP4HA2 and the reciprocal but outofframe P4HA2TBCK fusion transcripts. PMID: 27633981
    3. We have reported a series of 13 individuals from nine unrelated families that harbor biallelic mutation in TBCK and display overlapping features of intellectual disability and hypotonia. This condition is called TBCK-related intellectual disability syndrome. PMID: 27040691
    4. We have established that biallelic mutations in TBCK cause a severe neurodevelopmental disorder whose major features include profound developmental delay or cognitive deficit, brain atrophy without microcephaly. PMID: 27040692
    5. localization and function of TBCK PMID: 24576458
    6. TBCK may play an important role in cell proliferation, cell growth and actin organization possibly by modulating mTOR pathway. PMID: 23977024

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  • 相關(guān)疾?。?/div>
    Hypotonia, infantile, with psychomotor retardation and characteristic facies 3 (IHPRF3)
  • 亞細(xì)胞定位:
    Cytoplasm. Cytoplasm, cytoskeleton, spindle. Midbody.
  • 蛋白家族:
    Protein kinase superfamily
  • 數(shù)據(jù)庫(kù)鏈接:

    HGNC: 28261

    OMIM: 616899

    KEGG: hsa:93627

    STRING: 9606.ENSP00000273980

    UniGene: Hs.151498