Lipoprotein Lipase antibody (C-Term)

Catalog No. ABIN2788391

Product Details anti-Lipoprotein Lipase Antibody

Target: Lipoprotein Lipase (LPL)

Binding Specificity: C-Term

Reactivity: Human, Rat, Cow, Pig, Goat, Horse, Dog, Rabbit, Sheep

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Lipoprotein Lipase antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Sequence: LGYEINKVRA KRSSKMYLKT RSQMPYKVFH YQVKIHFSGT ESETHTNQAF

Predicted Reactivity: Cow: 86%, Dog: 79%, Goat: 86%, Horse: 86%, Human: 100%, Pig: 92%, Rabbit: 86%, Rat: 86%, Sheep: 86%

Characteristics: This is a rabbit polyclonal antibody against LPL. It was validated on Western Blot.

Purification: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the C terminal region of human LPL

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator.

Comment:

Antigen size: 475 AA

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Preservative: Sodium azide

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

Handling Advice: Avoid repeated freeze-thaw cycles.

Storage: -20 °C

Storage Comment: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Target Details for Lipoprotein Lipase

Target: Lipoprotein Lipase (LPL)

Alternative Name: LPL (LPL Products)

Synonyms: HDLCQ11 antibody, LIPD antibody, fb62e04 antibody, fc49b03 antibody, wu:fb62e04 antibody, wu:fc49b03 antibody, LPL antibody, lipd antibody, hdlcq11 antibody, lpl antibody, LOC100223817 antibody, lipoprotein lipase antibody, LPL antibody, Lpl antibody, lpl antibody

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.
Alias Symbols: HDLCQ11, LIPD
Protein Interaction Partner: LMF1, LPL, CALR, CCND1, APP, CUL3, UBC, PLK1, LUC7L2, KIAA1377, COPS6, ASCC2, RPL18A, UBE2Z, APOC2, LRP2, VLDLR, PTPN4, CETP, LRP1, EMD,
Protein Size: 475

Molecular Weight: 50 kDa

Gene ID: 4023

NCBI Accession: NM_000237, NP_000228

UniProt: P06858

Pathways: Lipid Metabolism