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Lipoprotein Lipase 抗体 (AA 300-327)

LPL 适用: 人 WB, IHC, ELISA, FACS 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN3031635
发货至: 中国
  • 抗原 See all Lipoprotein Lipase (LPL) 抗体
    Lipoprotein Lipase (LPL)
    抗原表位
    • 16
    • 8
    • 5
    • 5
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 300-327
    适用
    • 80
    • 30
    • 21
    • 19
    • 7
    • 7
    • 5
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    宿主
    • 61
    • 24
    • 2
    克隆类型
    • 56
    • 32
    多克隆
    标记
    • 39
    • 8
    • 7
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Lipoprotein Lipase antibody is un-conjugated
    应用范围
    • 66
    • 32
    • 29
    • 21
    • 18
    • 14
    • 14
    • 8
    • 7
    • 6
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Flow Cytometry (FACS)
    交叉反应 (详细)
    Expected species reactivity: Mouse, Rat, Bovine, Pig
    纯化方法
    Antigen affinity purified
    免疫原
    A portion of amino acids 300-327 from the human protein was used as the immunogen for this LPL antibody.
    亚型
    Ig Fraction
    Top Product
    Discover our top product LPL Primary Antibody
  • 应用备注
    Titration of the LPL antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000,IHC (Paraffin): 1:10-1:50,Flow Cytometry: 1:10-1:50
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    In 1X PBS, pH 7.4, with 0.09 % 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
    -20 °C
    储存方法
    Aliquot the LPL antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • 抗原
    Lipoprotein Lipase (LPL)
    别名
    LPL (LPL 产品)
    背景
    LPL encodes lipoprotein lipase, which is expressed in heart, muscle, and adipose tissue. LPL functions as a homodimer, and has the dual functions of triglyceride hydrolase and ligand/bridging factor for receptor-mediated lipoprotein uptake. Severe mutations that cause LPL deficiency result in type I hyperlipoproteinemia, while less extreme mutations in LPL are linked to many disorders of lipoprotein metabolism. [provided by RefSeq].
    UniProt
    P06858
    途径
    Lipid Metabolism
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