电话:
400-7060-959
传真:
+86 10 56315212-8813
电子邮件:
orders@antibodies-online.cn

INPP5E 抗体 (Middle Region)

INPP5E 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN5516992
发货至: 中国
  • 抗原 See all INPP5E 抗体
    INPP5E (Inositol Polyphosphate-5-Phosphatase, 72 KDa (INPP5E))
    抗原表位
    • 4
    • 3
    • 2
    • 1
    Middle Region
    适用
    • 19
    • 10
    • 10
    宿主
    • 17
    • 2
    克隆类型
    • 19
    多克隆
    标记
    • 9
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This INPP5E antibody is un-conjugated
    应用范围
    • 8
    • 6
    • 4
    • 3
    • 1
    Western Blotting (WB)
    序列
    SLQEIPKSRG VLSSERGSPS SGGNPLSGVA SSSPNLPHRD AAVAGSSPRL
    纯化方法
    Affinity purified
    免疫原
    The immunogen is a synthetic peptide directed towards the middle region of human INPP5E
    Top Product
    Discover our top product INPP5E Primary Antibody
  • 应用备注
    Optimal working dilution should be determined by the investigator.
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    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
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • 抗原
    INPP5E (Inositol Polyphosphate-5-Phosphatase, 72 KDa (INPP5E))
    别名
    INPP5E (INPP5E 产品)
    别名
    1200002L24Rik antibody, 72kDa antibody, mKIAA0123 antibody, CORS1 antibody, CPD4 antibody, JBTS1 antibody, MORMS antibody, PPI5PIV antibody, PMPCA antibody, inositol polyphosphate-5-phosphatase E antibody, Inpp5e antibody, INPP5E antibody
    背景
    The protein encoded by this gene is an inositol 1,4,5-trisphosphate (InsP3) 5-phosphatase. InsP3 5-phosphatases hydrolyze Ins(1,4,5)P3, which mobilizes intracellular calcium and acts as a second messenger mediating cell responses to various stimulation. Studies of the mouse counterpart suggest that this protein may hydrolyze phosphatidylinositol 3,4,5-trisphosphate and phosphatidylinositol 3,5-bisphosphate on the cytoplasmic Golgi membrane and thereby regulate Golgi-vesicular trafficking. Mutations in this gene cause Joubert syndrome, a clinically and genetically heterogenous group of disorders characterized by midbrain-hindbrain malformation and various associated ciliopathies that include retinal dystrophy, nephronophthisis, liver fibrosis and polydactyly. Alternative splicing results in multiple transcript variants encoding different isoforms.

    Alias Symbols: CPD4, CORS1, JBTS1, MORMS, PPI5PIV

    Protein Size: 610
    基因ID
    56623
    NCBI登录号
    NM_019892, NP_063945
You are here:
客服