Lipoprotein Lipase anticorps (C-Term)

N° du produit ABIN2788391

L’anticorps Lapin Polyclonal anti-Lipoprotein Lipase a été validé pour WB et IHC. Il convient pour détecter Lipoprotein Lipase dans des échantillons de Humain, Rat, Boeuf (Vache), Porc, Chévre, Cheval, Chien, Lapin et Mouton.

Aperçu rapide pour Lipoprotein Lipase anticorps (C-Term) (ABIN2788391)

Antigène: Lipoprotein Lipase (LPL)

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

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Lipoprotein Lipase est non-conjugé

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

Détail du produit anti-Lipoprotein Lipase anticorps

Épitope: C-Term

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

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