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AFF2 抗体 (AA 886-912)

AFF2 适用: 人 WB 宿主: 兔 Polyclonal RB24533 unconjugated
产品编号 ABIN1538678
发货至: 中国
  • 抗原 See all AFF2 抗体
    AFF2 (AF4/FMR2 Family, Member 2 (AFF2))
    抗原表位
    • 15
    • 6
    • 6
    • 6
    • 6
    • 5
    • 2
    • 1
    • 1
    • 1
    AA 886-912
    适用
    • 46
    • 10
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    宿主
    • 45
    • 1
    克隆类型
    • 45
    • 1
    多克隆
    标记
    • 11
    • 5
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This AFF2 antibody is un-conjugated
    应用范围
    • 35
    • 22
    • 13
    • 13
    • 3
    • 3
    • 2
    • 1
    Western Blotting (WB)
    纯化方法
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    免疫原
    This AFF2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 886-912 amino acids from the Central region of human AFF2.
    克隆位点
    RB24533
    亚型
    Ig Fraction
    Top Product
    Discover our top product AFF2 Primary Antibody
  • 应用备注
    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
    AFF2 Antibody (Center) 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
    AFF2 (AF4/FMR2 Family, Member 2 (AFF2))
    别名
    AFF2 (AFF2 产品)
    别名
    FMR2 antibody, FMR2P antibody, FRAXE antibody, MRX2 antibody, OX19 antibody, Fmr2 antibody, Ox19 antibody, Oxh antibody, AF4/FMR2 family member 2 antibody, AF4/FMR2 family, member 2 antibody, AFF2 antibody, Aff2 antibody
    背景
    This gene encodes a putative transcriptional activator that is a member of the AF4FMR2 gene family. This gene is associated with the folate-sensitive fragile X E locus on chromosome X. A repeat polymorphism in the fragile X E locus results in silencing of this gene causing Fragile X E syndrome. Fragile X E syndrome is a form of nonsyndromic X-linked mental retardation. Alternate splicing results in multiple transcript variants.
    分子量
    144771
    基因ID
    2334
    NCBI登录号
    NP_001162593, NP_001162594, NP_001162595, NP_001162596, NP_001164099, NP_002016
    UniProt
    P51816
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