Lipoprotein Lipase 抗体 (Center)
Quick Overview for Lipoprotein Lipase 抗体 (Center) (ABIN2798466)
抗原
See all Lipoprotein Lipase (LPL) 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 300-327, Center
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原理
- Rabbit Anti-Human LPL (Center) Antibody
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免疫原
- This LPL antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 300-327 amino acids from the Central region of human LPL.
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亚型
- Ig Fraction
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anti-Lipoprotein Lipase (LPL) (AA 28-474) antibody
LPL 适用: 大鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Lipoprotein Lipase (LPL) (AA 300-327) antibodyLPL 适用: 人 WB, IHC, ELISA, FACS 宿主: 兔 Polyclonal unconjugated
anti-Lipoprotein Lipase (LPL) (AA 55-316) antibodyLPL 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Lipoprotein Lipase (LPL) antibodyLPL 适用: 人 WB, ICC, IF, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Lipoprotein Lipase (LPL) (AA 162-246) antibodyLPL 适用: 人 IHC, ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Lipoprotein Lipase (LPL) antibody (HRP)LPL 适用: 人, 大鼠, Cow, 小鸡, 豚鼠 WB, IP, ELISA 宿主: 小鼠 Monoclonal 5D2 HRP
anti-Lipoprotein Lipase (LPL) (AA 1-475) antibodyLPL 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
anti-Lipoprotein Lipase (LPL) antibodyLPL 适用: 人, 大鼠, 小鼠, Golden Syrian Hamster, Cat WB, ELISA, FACS, IF, InhA 宿主: 小鼠 Monoclonal 5D2 unconjugated
anti-Lipoprotein Lipase (LPL) antibodyLPL 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 2C5 unconjugated
anti-Lipoprotein Lipase (LPL) (AA 300-327) antibodyLPL 适用: 人 WB, FACS, IHC (p) 宿主: 兔 Polyclonal unconjugated
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应用备注
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Western Blot, Immunohistochemistry, Flow Cytometry
Recommended Dilutions
WB: 1:1000, IHC: 1:10-50, FC: 1:10-50LPL Antibody (Center) .FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis. -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.5 mg/mL
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储存条件
- 4 °C,-20 °C
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储存方法
- 2-8°C (short-term), -20°C (long-term)
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- Lipoprotein Lipase (LPL)
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别名
- LPL
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背景
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Target Description: 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].
Gene Symbol: LPL
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分子量
- 53162 Da
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基因ID
- 4023
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UniProt
- P06858
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途径
- Lipid Metabolism
抗原
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