LOR anticorps (N-Term)

N° du produit ABIN629750

L’anticorps anti-LOR Polyclonal Lapin est utilisé pour la détection de LOR. Il a été validé pour WB et IHC.

Aperçu rapide pour LOR anticorps (N-Term) (ABIN629750)

Antigène: LOR (Loricrin (LOR))

Reactivité: Veuillez nous consulter SVP

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp LOR est non-conjugé

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

Détail du produit anti-LOR anticorps

Épitope: N-Term

Specificité: Loricrin antibody was raised against the N terminal of LOR

Purification: Purified

Immunogène: Loricrin antibody was raised using the N terminal of LOR corresponding to a region with amino acids GYSGGGCGGGSSGGGGGGGIGGCGGGSGGSVKYSGGGGSSGGGSGCFSSG

Information d'application

Indications d'application: WB: 5 µg/mL, IHC: 4-8 µg/mL
Optimal conditions should be determined by the investigator.

Commentaires:

Loricrin Blocking Peptide, (ABIN939071), is also available for use as a blocking control in assays to test for specificity of this Loricrin antibody

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Lyophilized powder. Add distilled water for a 1 mg/mL concentration of LOR 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 LOR

Antigène: LOR (Loricrin (LOR))

Autre désignation: Loricrin

Classe de substances: Chemical

Sujet: LOR is a major protein component of the cornified cell envelope found in terminally differentiated epidermal cells. Mutations in this gene are associated with Vohwinkel's syndrome and progressive symmetric erythrokeratoderma, both inherited skin diseases.LOR encodes loricrin, a major protein component of the cornified cell envelope found in terminally differentiated epidermal cells. Mutations in LOR may be the cause of both Vohwinkel's syndrome and progressive symmetric erythrokeratoderma, both inherited skin diseases.

Poids moléculaire: 35 kDa (MW of target protein)