Invitrogen

LPL Polyclonal Antibody

LPL Antibody in Immunohistochemistry (Paraffin) (IHC (P))

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LPL Antibody (PA5-34812) in IHC (P)

LPL Polyclonal Antibody detects secreted LPL protein by immunohistochemical analysis. Sample: Paraffin-embedded mouse white adipocyte. LPL stained by LPL Polyclonal Antibody (Product # PA5-34812) diluted at 1:500. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min.

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产品信息

PA5-34812

应用

建议稀释比

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免疫印迹 (WB)

1:500-1:3,000

免疫组化（石蜡） (IHC (P))

Assay-dependent

产品规格

种属反应

Mouse

宿主/亚型

Rabbit / IgG

分类

Polyclonal

类型

Antibody

抗原

Recombinant protein fragment contains a sequence corresponding to a region within amino acids 134 and 354 (P06858) of LPL

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偶联物

Unconjugated Unconjugated Unconjugated

形式

Liquid

浓度

1.35 mg/mL

纯化类型

Antigen affinity chromatography

保存液

PBS, pH 7, with 20% glycerol

内含物

0.025% ProClin 300

保存条件

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

运输条件

Wet ice

AB_2552164

产品详细信息

Recommended positive controls: A431, H1299, HeLa, Molt-4.

Predicted reactivity: Human (99%), Mouse (96%), Rat (95%), Cat (97%), Pig (96%), Rabbit (96%), Chicken (80%), Sheep (96%), Bovine (96%), Guinea pig (90%).

Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.

靶标信息

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.

仅用于科研。不用于诊断过程。未经明确授权不得转售。