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

TBC1D22A 抗体

TBC1D22A 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7131302
发货至: 中国
  • 抗原 See all TBC1D22A 抗体
    TBC1D22A (TBC1 Domain Family, Member 22A (TBC1D22A))
    适用
    • 34
    • 5
    • 5
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    宿主
    • 34
    克隆类型
    • 34
    多克隆
    标记
    • 14
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This TBC1D22A antibody is un-conjugated
    应用范围
    • 24
    • 18
    • 14
    • 3
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    交叉反应
    人, 小鼠
    纯化方法
    Antigen affinity purification
    免疫原
    Fusion protein of Human TBC1D22A
    亚型
    IgG
    Top Product
    Discover our top product TBC1D22A Primary Antibody
  • 应用备注
    ELISA:1:2000-1:5000, IHC:1:25-1:100,
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
    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,-80 °C
    储存方法
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 抗原
    TBC1D22A (TBC1 Domain Family, Member 22A (TBC1D22A))
    别名
    TBC1D22A (TBC1D22A 产品)
    别名
    C22orf4 antibody, HSC79E021 antibody, BC023106 antibody, D15Ertd781e antibody, RGD1306588 antibody, TBC1 domain family member 22A antibody, TBC1 domain family, member 22a antibody, TBC1D22A antibody, Tbc1d22a antibody
    背景

    Background: TBC1D22A (TBC1 domain family, member 22A), also known as C22orf4, is a 517 amino acid protein that contains one Rab-GAP TBC domain and is thought to function as a GTPase-activating protein for Rab family members. Multiple isoforms of TBC1D22A exist due to alternative splicing events. The gene encoding TBC1D22A maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.

    Aliases: TBC1D22A antibody, C22orf4 antibody, TBC1 domain family member 22A antibody

    UniProt
    Q8WUA7
You are here: