Anti-LPL

• 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, Jul 2008]

• Immunogen:

  Human LPL whole protein

• Clonality:

  Monoclonal

• Clone:

  LPL.A4

• Type:

  Antibodies-Monoclonal

• Applications:

  WB,ELISA

• Concentration:

  100ug/100ul

• Buffer:

  PBS, pH 7.4 with 0.05% sodium azide.

• Shipping Conditions:

  Ice Pack

• Storage Conditions:

  This product is stable for several weeks at 4° C as an undiluted liquid. Dilute only prior to immediate use. For extended storage, aliquot contents and freeze at -20° C or below. Avoid cycles of freezing and thawing. Expiration date is one (1) year from date of receipt.

• Fragment:

  IgG

• Specificity:

  Specifically recognizes Lipoprotein Lipase (LPL) from human and bovine.

• CAS Number:

  9007-83-4