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Septin 5 Protein (SEPT5) (Myc-DYKDDDDK Tag)

SEPT5 宿主: 人 宿主: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
产品编号 ABIN2731689
发货至: 中国
  • 抗原 See all Septin 5 (SEPT5) 蛋白
    Septin 5 (SEPT5)
    蛋白类型
    Recombinant
    宿主
    • 5
    • 2
    • 1
    资源
    • 3
    • 2
    • 1
    HEK-293 Cells
    标记
    This Septin 5 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human Septin-5 (SEPT5) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    纯度
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product SEPT5 蛋白
  • 应用备注
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    说明

    The tag is located at the C-terminal.

    限制
    仅限研究用
  • 浓度
    50 μg/mL
    缓冲液
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    储存条件
    -80 °C
    储存方法
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • 抗原
    Septin 5 (SEPT5)
    别名
    Septin-5 (Sept5) (SEPT5 产品)
    别名
    sept5 Protein, fj37h04 Protein, zgc:73218 Protein, wu:fj37h04 Protein, SEPT5 Protein, Cdcrel-1 Protein, Cdcrel1 Protein, Pnutl1 Protein, 5-Sep Protein, CDCrel-1A Protein, CDCREL Protein, CDCREL-1 Protein, CDCREL1 Protein, H5 Protein, HCDCREL-1 Protein, PNUTL1 Protein, septin 5a Protein, septin 5 Protein, sept5a Protein, SEPT5 Protein, sept5 Protein, Sept5 Protein
    背景
    This gene is a member of the septin gene family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is mapped to 22q11, the region frequently deleted in DiGeorge and velocardiofacial syndromes. A translocation involving the MLL gene and this gene has also been reported in patients with acute myeloid leukemia. Alternative splicing results in multiple transcript variants. The presence of a non-consensus polyA signal (AACAAT) in this gene also results in read-through transcription into the downstream neighboring gene (GP1BB platelet glycoprotein Ib), whereby larger, non-coding transcripts are produced.
    分子量
    42.6 kDa
    NCBI登录号
    NP_002679
    途径
    Synaptic Vesicle Exocytosis
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