Lipase A anticorps (N-Term)

N° du produit ABIN2788678

Cet anticorps anti-Lipase A est un anticorps Lapin Polyclonal détectant Lipase A dans WB. Adapté pour Humain, Rat, Cheval, Porc, Boeuf (Vache), Lapin et Mouton.

Aperçu rapide pour Lipase A anticorps (N-Term) (ABIN2788678)

Antigène: Lipase A (LIPA) (Lipase A, Lysosomal Acid, Cholesterol Esterase (LIPA))

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

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Lipase A est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-Lipase A anticorps

Épitope: N-Term

Séquence: SYWGFPSEEY LVETEDGYIL CLNRIPHGRK NHSDKGPKPV VFLQHGLLAD

Homologie: Cow: 93%, Horse: 86%, Human: 100%, Pig: 100%, Rabbit: 93%, Rat: 86%, Sheep: 93%

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

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the N terminal region of human LIPA

Information d'application

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

Commentaires:

Antigen size: 399 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 Lipase A

Antigène: Lipase A (LIPA) (Lipase A, Lysosomal Acid, Cholesterol Esterase (LIPA))

Autre désignation: LIPA

Sujet: This gene encodes lipase A, the lysosomal acid lipase (also known as cholesterol ester hydrolase). This enzyme functions in the lysosome to catalyze the hydrolysis of cholesteryl esters and triglycerides. Mutations in this gene can result in Wolman disease and cholesteryl ester storage disease. Alternatively spliced transcript variants encoding the same protein have been found for this gene.
Alias Symbols: CESD, LAL
Protein Interaction Partner: ELAVL1, UBC,
Protein Size: 399

Poids moléculaire: 43 kDa

ID gène: 3988

NCBI Accession: NM_000235, NP_000226

UniProt: P38571