Lipoprotein Lipase anticorps (C-Term)

N° du produit ABIN2788391

Détail du produit anti-Lipoprotein Lipase anticorps

Antigène: Lipoprotein Lipase (LPL)

Épitope: C-Term

Reactivité: Humain, Rat, Boeuf (Vache), Porc, Chévre, Cheval, Lapin, Mouton, Chien

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Lipoprotein Lipase est non-conjugé

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

Séquence: LGYEINKVRA KRSSKMYLKT RSQMPYKVFH YQVKIHFSGT ESETHTNQAF

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

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

Purification: Affinity Purified

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

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator.

Commentaires:

Antigen size: 475 AA

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: Lot specific

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

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Conseil sur la manipulation: Avoid repeated freeze-thaw cycles.

Stock: -20 °C

Stockage commentaire: 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.

Détails sur Lipoprotein Lipase

Antigène: Lipoprotein Lipase (LPL)

Autre désignation: LPL (LPL Produits)

Synonymes: anticorps HDLCQ11, anticorps LIPD, anticorps fb62e04, anticorps fc49b03, anticorps wu:fb62e04, anticorps wu:fc49b03, anticorps LPL, anticorps lipd, anticorps hdlcq11, anticorps lpl, anticorps LOC100223817, anticorps lipoprotein lipase, anticorps LPL, anticorps Lpl, anticorps lpl

Sujet: 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

Poids moléculaire: 50 kDa

ID gène: 4023

NCBI Accession: NM_000237, NP_000228

UniProt: P06858

Pathways: Lipid Metabolism