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  • 产品名称:真核翻译起始因子4E结合蛋白1(EIF4EBP1)重组蛋白

  • 产品型号:EIF4EBP1
  • 产品厂商:蛋白/多肽/抗原
  • 产品价格:0
  • 折扣价格:0
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简单介绍:
真核翻译起始因子4E结合蛋白1(EIF4EBP1)重组蛋白蛋白质的不同在于其氨基酸的种类、数目、排列顺序和肽链空间结构的不同,蛋白质的氨基酸序列由对应基因所编码,空间结构决定于氨基酸序列本身,通过氢键或范德华力等作用力实现。蛋白质不仅具有**结构,还具有二级、三级结构,甚至四级结构。**结构只是蛋白质的基本结构,称之为低级结构。真核翻译起始因子4E结合蛋白1(EIF4EBP1)重组蛋白如果想让蛋白质有更多的生物功能则必须赋予它们更复杂的空间结构,称之为**结构。应用重组DNA将目标基因进行表达得到的
详情介绍:

真核翻译起始因子4E结合蛋白1(EIF4EBP1)重组蛋白

  • 物种Homo sapiens (Human,人)相同的名称,不同的物种。
  • 性状冻干粉内**水平<1.0EU/µg(LAL法测定)
  • 亚细胞定位n/a
  • 预测分子量13.9kDa
  • 实际分子量-(差异分析请参阅说明书)
  • 片段与标签Ser2-Ile118 (Accession # Q13541) with N-terminal His Tag
  • 缓冲液成份磷酸盐缓冲液(pH7.4,含有 0.01% SKL, 1mM DTT, 5% Trehalose和Proclin300.)
  • 纯度> 95%
  • 等电点-
  • 应用SDS-PAGE; WB; ELISA; I
    真核翻译起始因子4E结合蛋白1(EIF4EBP1)重组蛋白用法
    PBS或其它。
    储存
    避免反复冻融。2-8°C不超过一个月,-80°C不超过12个月。
    稳定性
    热稳定性以损失率显示。损失率是由加速降解试验决定,具体方法如下:在37°C孵育48小时,没有显著的降解或者沉淀产生。保质期内,在适当的条件下存储,损失率低于5%。
    真核翻译起始因子4E结合蛋白1(EIF4EBP1)重组蛋白


    Eukaryotic Eukaryotic Eukaryotic Eukaryotic Translation Translation Translation Translation Initiation Initiation Initiation Initiation Factor 4E Binding Binding Binding Binding Protein Protein Protein Protein 1 (EIF4EBP1) (EIF4EBP1) (EIF4EBP1) (EIF4EBP1)

    Organism: Organism: Organism: Organism: Homo sapiens sapiens sapiens sapiens (Human) (Human) (Human) (Human)

    Instruction Instruction Instruction Instruction manual

    FOR IN VITRO USE AND RESEARCH USE ONLY

    NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES

    1th Edition (Revised in February, 2012)

    真核翻译起始因子4E结合蛋白1(EIF4EBP1)重组蛋白[ DESCRIPTION DESCRIPTION DESCRIPTION DESCRIPTION ]

    Protein Protein Protein Protein Names: Eukaryotic Translation Initiation Factor 4E Binding Protein 1

    Gene Names: EIF4EBP1

    Size: 100µg

    Source: Recombinant

    Expression Expression Expression Expression Host: E.coli

    Function: Function: Function: Function: Regulates eIF4E activity by preventing its assembly into the eIF4F complex.

    Mediates the regulation of protein translation by hormones, growth factors and other

    stimuli that signal through the MAP kinase and mTORC1 pathways.

    Subcellular Subcellular Subcellular Subcellular Location: Location: Location: Location: Nucleus but not nucleoli, Cytoplasm

    Tissue Specificity: Specificity: Specificity: Specificity: Selective cytoplasmic expression in salivary gland, pancreas, the

    gastrointestinal tract and non-keratinized squamous epithelia.

    [ PROPERTIES ROPERTIES ROPERTIES ROPERTIES ]

    Residues Residues Residues Residues: Ser2-Ile118 (Accession # Q13541), with a N-terminal His-tag.

    Grade & Purity: Purity: Purity: Purity: >97%, 13.97 kDa as determined by SDS-PAGE reducing conditions.

    Form & Buffer: Supplied as lyophilized form in PBS, pH 7.4.

    Endotoxin Endotoxin Endotoxin Endotoxin Level: <1.0 EU per 1μg(determined by the LAL method). Applications: Applications: Applications: Applications: SDS-PAGE; WB; ELISA;IP.

    (May be suitable for use in other assays to be determined by the end user.)

    Predicted Predicted Predicted Predicted Molecular Molecular Molecular Molecular Mass: 13.97 kDa

    真核翻译起始因子4E结合蛋白1(EIF4EBP1)重组蛋白[ PREPARATION PREPARATION PREPARATION PREPARATION ]

    Reconstitute in PBS.

    [ STORAGE STORAGE STORAGE STORAGE AND STABILITY STABILITY STABILITY STABILITY ]

    Storage: Storage: Storage: Storage: Store at 4oC for short term storage (1-2 weeks). Aliquot and store at -20oC or -80oC for long term

    storage. Avoid repeated freeze/thaw cycles.

    Valid period: period: period: period: 12 months stored at -80oC.

    [ BACKGROUND BACKGROUND BACKGROUND BACKGROUND]

    The target protein is fused with a His-tag and its sequence is listed below. The first Met is an initiator amino acid. Moreover, Gly and Ser are added to improve the flexibility of N-terminus at both ends of the His-tag, which will

    increase the chelating ability of the tag to Ni-Sepharose during purification.

    MGHHHHHHSGSEF-SGGSSCSQT PSRAIPATRR VVLGDGVQLP PGDYSTTPGG TLFSTTPGGT RIIYDRKFLM

    ECRNSPVTKT PPRDLPTIPG VTSPSSDEPP MEASQSHLRN SPEDKRAGGE ESQFEMDI

    [ REFERENCES REFERENCES REFERENCES REFERENCES ]

    1. Schalm S.S., et al. (2003) Curr. Biol. 13:797-806. 2. Pause A., et al. (1994) Nature 371:762-767. 3. Ha, Sang Hoon, et al. (2006) Cell. Signal. (England) 18 (12): 2283–2291.

    4. Haghighat A., et al. (1995) EMBO J. 14:5701-5709. 5. Hara K., et al. (2002) Cell 110:177-189.


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