Kyphoscoliosis Peptidase anticorps (AA 51-150)

N° du produit ABIN1386443

L’anticorps Lapin Polyclonal anti-Kyphoscoliosis Peptidase a été validé pour WB, ELISA, IHC (fro), IF (cc), IF (p), ICC et IHC (p). Il convient pour détecter Kyphoscoliosis Peptidase dans des échantillons de Humain.

Aperçu rapide pour Kyphoscoliosis Peptidase anticorps (AA 51-150) (ABIN1386443)

Antigène: Kyphoscoliosis Peptidase (KY)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Kyphoscoliosis Peptidase est non-conjugé

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunocytochemistry (ICC), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-Kyphoscoliosis Peptidase anticorps

Épitope: AA 51-150

Homologie: Human,Mouse,Rat,Dog,Pig

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human Kyphoscoliosis peptidase

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

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

Stock: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur Kyphoscoliosis Peptidase

Antigène: Kyphoscoliosis Peptidase (KY)

Autre désignation: KY/Kyphoscoliosis peptidase

Sujet:

Synonyms: KY, KY_HUMAN, Kyphoscoliosis peptidase.

Background: KY peptidase (Kyphoscoliosis peptidase) is a 561 amino acid cytoskeleton protease that interacts with several sarcomeric cytoskeletal proteins, including Filamin 2. KY peptidase probably plays a role in the maturation, function and stabilization of the neuromuscular junction. KY-null mouse mutants exhibit distinct irregular subceullular Filamin 2 localization, suggesting that KY peptidase deficiency may be the cause of several types of limb-girdle muscular dystrophies.

ID gène: 339855

Pathways: Skeletal Muscle Fiber Development