Product overview:

LPL (Lipoprotein lipase) mouse monoclonal antibody, clone LBI4G7

Field of research:

Alzheimer's disease, Glycerolipid metabolism, PPAR signaling pathway

Summary:

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]

Alternative names:

HDLCQ11; LIPD

Species reactivity:

Human, Mouse, Rat

Host:

Mouse

Target:

LPL

Isotype:

IgG1

Immunogen:

Human recombinant protein fragment corresponding to amino acids 28-475 of human LPL(NP_000228) produced in HEK293T cell.

Clone:

LBI4G7

Conjugation:

Unconjugated

Gene name:

lipoprotein lipase

Symbol:

LPL

Pathway:

Alzheimer's disease, Glycerolipid metabolism, PPAR signaling pathway

Function:

Druggable Genome

Purification:

Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)

Concentration:

0.82 mg/ml

Form:

PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.

Applications & dilution:

WB 1:2000, IHC 1:150, IF 1:100

Storage buffer:

PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.

Storage:

Store at +4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

More info:

Email: info@sobekbio.com

Orders:

Email: orders@sobekbio.com