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CRYM 抗体

CRYM 适用: 人, 小鼠, 大鼠 IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7260867
发货至: 中国
  • 抗原 See all CRYM 抗体
    CRYM (Crystallin, mu (CRYM))
    适用
    • 24
    • 11
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 23
    • 7
    克隆类型
    • 24
    • 6
    多克隆
    标记
    • 21
    • 3
    • 2
    • 2
    • 1
    • 1
    This CRYM antibody is un-conjugated
    应用范围
    • 24
    • 14
    • 8
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human CRYM (NP_001879.1).
    亚型
    IgG
    Top Product
    Discover our top product CRYM Primary Antibody
  • 应用备注
    IHC 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    CRYM (Crystallin, mu (CRYM))
    别名
    CRYM (CRYM 产品)
    别名
    CRYM antibody, zgc:158843 antibody, DFNA40 antibody, THBP antibody, crystallin mu antibody, crystallin, mu antibody, Cro/Cl family transcriptional regulator antibody, crystallin mu L homeolog antibody, CRYM antibody, crym antibody, EAMY_RS27495 antibody, crym.L antibody, Crym antibody
    背景
    Crystallins are separated into two classes: taxon-specific and ubiquitous. The former class is also called phylogenetically-restricted crystallins. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. This gene encodes a taxon-specific crystallin protein that binds NADPH and has sequence similarity to bacterial ornithine cyclodeaminases. The encoded protein does not perform a structural role in lens tissue, and instead it binds thyroid hormone for possible regulatory or developmental roles. Mutations in this gene have been associated with autosomal dominant non-syndromic deafness.
    基因ID
    1428
    UniProt
    Q14894
    途径
    Hormone Transport, Sensory Perception of Sound
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