Kyphoscoliosis Peptidase anticorps (AA 51-150) (Alexa Fluor 488)

N° du produit ABIN1389712

Détail du produit anti-Kyphoscoliosis Peptidase anticorps (Alexa Fluor 488)

Antigène: Kyphoscoliosis Peptidase (KY)

Épitope: AA 51-150

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Kyphoscoliosis Peptidase est conjugé à/à la Alexa Fluor 488

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

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: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur Kyphoscoliosis Peptidase

Antigène: Kyphoscoliosis Peptidase (KY)

Autre désignation: KY/Kyphoscoliosis peptidase (KY Produits)

Synonymes: anticorps CD1, anticorps D9Mgc44e, anticorps ky, anticorps kyphoscoliosis peptidase, anticorps Ky, anticorps KY

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