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

VMA21 抗体

VMA21 适用: 人, 小鼠 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7254226
发货至: 中国
  • 抗原 See all VMA21 抗体
    VMA21 (Vacuolar H+-ATPase Homolog (VMA21))
    适用
    • 13
    • 11
    • 2
    • 2
    • 1
    • 1
    • 1
    人, 小鼠
    宿主
    • 13
    克隆类型
    • 13
    多克隆
    标记
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This VMA21 antibody is un-conjugated
    应用范围
    • 6
    • 3
    • 3
    • 2
    • 1
    ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF)
    产品特性
    Polyclonal Antibody
    纯化方法
    Antigen affinity purification
    免疫原
    Synthetic peptide of human VMA21
    亚型
    IgG
  • 应用备注
    IHC 1:150-1:500, IF 1: 50-1:200, ELISA 1:5000-1:240000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    2.6 mg/mL
    缓冲液
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    VMA21 (Vacuolar H+-ATPase Homolog (VMA21))
    别名
    VMA21 (VMA21 产品)
    别名
    MEAX antibody, XMEA antibody, ATP6H antibody, ATP6V0E antibody, M9.2 antibody, Vma21 antibody, Vma21p antibody, RGD1566155 antibody, 2610030H06Rik antibody, AI840175 antibody, VMA21, vacuolar ATPase assembly factor antibody, ATPase H+ transporting V0 subunit e1 antibody, VMA21 vacuolar H+-ATPase homolog (S. cerevisiae) antibody, VMA21, vacuolar ATPase assembly factor L homeolog antibody, VMA21 antibody, ATP6V0E1 antibody, Vma21 antibody, vma21.L antibody
    背景
    This gene encodes a chaperone for assembly of lysosomal vacuolar ATPase. Required for the assembly of the V0 complex of the vacuolar ATPase (V-ATPase) in the endoplasmic reticulum. Associates with the V0 complex of the vacuolar ATPase (V-ATPase). MEAX is a childhood-onset disease characterized by progressive vacuolation and atrophy of skeletal muscle. It is inherited in recessive fashion, affecting boys and sparing carrier females. Onset is in childhood, and patients exhibit weakness of the proximal muscles of the lower extremities, progressing slowly to involve other skeletal muscle groups over time.
    UniProt
    Q3ZAQ7
You are here:
客服