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KLC2 抗体 (AA 1-90)

KLC2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7268140
发货至: 中国
  • 抗原 See all KLC2 抗体
    KLC2 (Kinesin Light Chain 2 (KLC2))
    抗原表位
    • 15
    • 8
    • 8
    • 8
    • 8
    • 7
    • 6
    • 2
    • 1
    AA 1-90
    适用
    • 56
    • 19
    • 15
    • 15
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    宿主
    • 54
    • 2
    克隆类型
    • 56
    多克隆
    标记
    • 16
    • 5
    • 5
    • 5
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This KLC2 antibody is un-conjugated
    应用范围
    • 49
    • 29
    • 28
    • 27
    • 13
    • 13
    • 8
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    原理
    KLC2 Rabbit pAb
    序列
    MAMMVFPREE KLSQDEIVLG TKAVIQGLET LRGEHRALLA PLVAPEAGEA EPGSQERCIL LRRSLEAIEL GLGEAQVILA LSSHLGAVES
    交叉反应
    人, 小鼠, 大鼠
    产品特性
    Polyclonal Antibodies
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein containing a sequence corresponding to amino acids 1-90 of human KLC2 (NP_073733.1).
    亚型
    IgG
    Top Product
    Discover our top product KLC2 Primary Antibody
  • 应用备注
    WB,1:500 - 1:2000
    限制
    仅限研究用
  • 状态
    Liquid
    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
    KLC2 (Kinesin Light Chain 2 (KLC2))
    别名
    KLC2 (KLC2 产品)
    别名
    MGC143149 antibody, wu:fc15b01 antibody, wu:fj62c06 antibody, zgc:162288 antibody, DKFZp459K0951 antibody, 8030455F02Rik antibody, AW212649 antibody, KLC 2 antibody, KLC-2 antibody, kinesin light chain 2 antibody, KLC2 antibody, klc2 antibody, Klc2 antibody
    背景
    The protein encoded by this gene is a light chain of kinesin, a molecular motor responsible for moving vesicles and organelles along microtubules. Defects in this gene are a cause of spastic paraplegia, optic atrophy, and neuropathy (SPOAN) syndrome. [provided by RefSeq, Mar 2016],KLC2,SPOAN,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Motor Proteins,KLC2
    分子量
    60kDa/68kDa
    基因ID
    64837
    UniProt
    Q9H0B6
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