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Septin 5 抗体

SEPT5 适用: 人, 大鼠, 小鼠 IHC, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7256500
发货至: 中国
  • 抗原 See all Septin 5 (SEPT5) 抗体
    Septin 5 (SEPT5)
    适用
    • 58
    • 30
    • 13
    • 2
    人, 大鼠, 小鼠
    宿主
    • 50
    • 8
    克隆类型
    • 50
    • 7
    • 1
    多克隆
    标记
    • 24
    • 5
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This Septin 5 antibody is un-conjugated
    应用范围
    • 52
    • 29
    • 26
    • 13
    • 13
    • 7
    • 6
    • 6
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human 44079 (NP_002679.2).
    亚型
    IgG
    Top Product
    Discover our top product SEPT5 Primary Antibody
  • 应用备注
    IHC 1:100-1:200 IF 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    Septin 5 (SEPT5)
    别名
    SEPT5 (SEPT5 产品)
    别名
    sept5 antibody, fj37h04 antibody, zgc:73218 antibody, wu:fj37h04 antibody, SEPT5 antibody, Cdcrel-1 antibody, Cdcrel1 antibody, Pnutl1 antibody, 5-Sep antibody, CDCrel-1A antibody, CDCREL antibody, CDCREL-1 antibody, CDCREL1 antibody, H5 antibody, HCDCREL-1 antibody, PNUTL1 antibody, septin 5a antibody, septin 5 antibody, sept5a antibody, SEPT5 antibody, sept5 antibody, Sept5 antibody
    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.
    基因ID
    5413
    UniProt
    Q99719
    途径
    Synaptic Vesicle Exocytosis
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