Kyphoscoliosis Peptidase antibody (AA 51-150) (Biotin)

Catalog No. ABIN1389715

This Rabbit Polyclonal antibody specifically detects Kyphoscoliosis Peptidase in WB, ELISA, IHC (fro) and IHC (p). It exhibits reactivity toward Human.

Quick Overview for Kyphoscoliosis Peptidase antibody (AA 51-150) (Biotin) (ABIN1389715)

Target: Kyphoscoliosis Peptidase (KY)

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Kyphoscoliosis Peptidase antibody is conjugated to Biotin

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-Kyphoscoliosis Peptidase Antibody (Biotin)

Binding Specificity: AA 51-150

Predicted Reactivity: Human,Mouse,Rat,Dog,Pig

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human Kyphoscoliosis peptidase

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Handling

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.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for Kyphoscoliosis Peptidase

Target: Kyphoscoliosis Peptidase (KY)

Alternative Name: KY/Kyphoscoliosis peptidase

Background:

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.

Gene ID: 339855

Pathways: Skeletal Muscle Fiber Development