ABHD5 anticorps (C-Term)

N° du produit ABIN632415

Cet anticorps anti-ABHD5 est un anticorps Lapin Polyclonal détectant ABHD5 dans WB. Adapté pour Humain, Souris et Rat.

Aperçu rapide pour ABHD5 anticorps (C-Term) (ABIN632415)

Antigène: ABHD5 (Abhydrolase Domain Containing 5 (ABHD5))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ABHD5 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-ABHD5 anticorps

Épitope: C-Term

Specificité: ABHD5 antibody was raised against the C terminal of ABHD5

Purification: Affinity purified

Immunogène: ABHD5 antibody was raised using the C terminal of ABHD5 corresponding to a region with amino acids SVIFGARSCIDGNSGTSIQSLRPHSYVKTIAILGAGHYVYADQPEEFNQK

Information d'application

Indications d'application: WB: 1 µg/mL
Optimal conditions should be determined by the investigator.

Commentaires:

ABHD5 Blocking Peptide, (ABIN5611866), is also available for use as a blocking control in assays to test for specificity of this ABHD5 antibody

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Lyophilized powder. Add distilled water for a 1 mg/mL concentration of ABHD5 antibody in PBS

Concentration: Lot specific

Buffer: PBS

Conseil sur la manipulation: Avoid repeated freeze/thaw cycles.
Dilute only prior to immediate use.

Stock: 4 °C/-20 °C

Stockage commentaire: Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.

Détails sur ABHD5

Antigène: ABHD5 (Abhydrolase Domain Containing 5 (ABHD5))

Autre désignation: ABHD5

Sujet: ABHD5 belongs to a large family of proteins defined by an alpha/beta hydrolase fold, and contains three sequence motifs that correspond to a catalytic triad found in the esterase/lipase/thioesterase subfamily. It differs from other members of this subfamily in that its putative catalytic triad contains an asparagine instead of the serine residue. Mutations in this gene have been associated with Chanarin-Dorfman syndrome, a triglyceride storage disease with impaired long-chain fatty acid oxidation.

Poids moléculaire: 38 kDa (MW of target protein)

Pathways: Lipid Metabolism