Search Thermo Fisher Scientific
Disclaimer
Clicking the images or links will redirect you to a website hosted by BenchSci that provides third-party scientific content. Neither the content nor the BenchSci technology and processes for selection have been evaluated by us; we are providing them as-is and without warranty of any kind, including for use or application of the Thermo Fisher Scientific products presented.
FIGURE: 1 / 4
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.
Product Details
PA5-34812
Applications
Tested Dilution
Publications
Product Specifications
Species Reactivity
Mouse
Host/Isotype
Rabbit
/ IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant protein fragment contains a sequence corresponding to a region within amino acids 134 and 354 (P06858) of LPL
Conjugate
Form
Liquid
Concentration
1.35 mg/mL
Purification
Antigen affinity chromatography
Storage buffer
PBS, pH 7, with 20% glycerol
Contains
0.025% ProClin 300
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Wet ice
RRID
AB_2552164
Product Specific Information
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.
Target Information
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
References (0)
Have you cited this product in a publication?
Let us know so we can reference it here.
Bioinformatics
Protein Aliases: alpha lipase; Lipoprotein lipase; LPL; O 1-4-5; Phospholipase A1
Gene Aliases: Lpl
UniProt ID: (Mouse) P11152
Entrez Gene ID: (Mouse) 16956
lipid metabolic process
fatty acid biosynthetic process
positive regulation of macrophage derived foam cell differentiation
positive regulation of cholesterol storage
positive regulation of sequestering of triglyceride
lipid catabolic process
triglyceride biosynthetic process
triglyceride catabolic process
very-low-density lipoprotein particle remodeling
triglyceride homeostasis
Performance Guarantee
If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
Learn more
We're here to help
Get expert recommendations for common problems or connect directly with an on staff expert for technical assistance related to applications, equipment and general product use.
Contact tech support