Lipoprotein Lipase antibody (AA 300-327)

Catalog No. ABIN5531554

This anti-Lipoprotein Lipase antibody is a Rabbit Polyclonal antibody detecting Lipoprotein Lipase in WB, FACS and IHC (p). Suitable for Human.

Quick Overview for Lipoprotein Lipase antibody (AA 300-327) (ABIN5531554)

Target: Lipoprotein Lipase (LPL)

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Lipoprotein Lipase antibody is un-conjugated

Application: Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-Lipoprotein Lipase Antibody

Binding Specificity: AA 300-327

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: 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.

Isotype: Ig Fraction

Application Details

Application Notes: For FACS starting dilution is: 1:25

For WB starting dilution is: 1:1000

For IHC-P starting dilution is: 1:10~50

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Target Details for Lipoprotein Lipase

Target: Lipoprotein Lipase (LPL)

Alternative Name: LPL

Background: 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].

Molecular Weight: 53 kDa

Gene ID: 4023

UniProt: P06858

Pathways: Lipid Metabolism