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Rho-related GTP-binding protein 抗体 (C-Term)

RhO (pan) 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal RB36659 unconjugated
产品编号 ABIN1537109
发货至: 中国
  • 抗原 See all Rho-related GTP-binding protein (RhO (pan)) 抗体
    Rho-related GTP-binding protein (RhO (pan))
    抗原表位
    • 8
    • 6
    • 5
    • 2
    • 1
    • 1
    • 1
    AA 310-339, C-Term
    适用
    • 17
    • 7
    • 7
    • 5
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 22
    • 4
    • 1
    克隆类型
    • 22
    • 5
    多克隆
    标记
    • 18
    • 3
    • 2
    • 2
    • 1
    • 1
    This Rho-related GTP-binding protein antibody is un-conjugated
    应用范围
    • 20
    • 18
    • 11
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    预测反应
    Pr
    纯化方法
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    免疫原
    This RHO antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 310-339 amino acids from the C-terminal region of human RHO.
    克隆位点
    RB36659
    亚型
    Ig Fraction
    Top Product
    Discover our top product RhO (pan) Primary Antibody
  • 应用备注
    WB: 1:2000. WB: 1:1000
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    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
    4 °C,-20 °C
    储存方法
    RHO Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
    有效期
    6 months
  • 抗原
    Rho-related GTP-binding protein (RhO (pan))
    别名
    RHO (RhO (pan) 产品)
    物质类
    Chemical
    背景
    Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive disorder. In the autosomal dominant form,which comprises about 25 % of total cases, approximately 30 % of families have mutations in the gene encoding the rod photoreceptor-specific protein rhodopsin. This is the transmembrane protein which, when photoexcited, initiates the visual transduction cascade. Defects in this gene are also one of the causes of congenital stationary night blindness.
    分子量
    38893
    基因ID
    6010
    NCBI登录号
    NP_000530
    UniProt
    P08100
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