MYOZ2 antibody

Catalog No. ABIN7252480

Product Details anti-MYOZ2 Antibody

Target: MYOZ2 (Myozenin 2 (MYOZ2))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MYOZ2 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Characteristics: Polyclonal Antibody

Purification: Antigen affinity purification

Immunogen: Full length fusion protein

Isotype: IgG

Application Details

Application Notes: WB 1:500-1:2000, ELISA 1:5000-1:10000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1.08 mg/mL

Buffer: PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

Preservative: Sodium azide

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

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for MYOZ2

Target: MYOZ2 (Myozenin 2 (MYOZ2))

Alternative Name: MYOZ2 (MYOZ2 Products)

Synonyms: LOC733663 antibody, myoz2 antibody, MGC52797 antibody, cs-1 antibody, myozenin-2 antibody, MYOZ2 antibody, Myozenin-2 antibody, DKFZp468M0519 antibody, 1110012I24Rik antibody, Fatz-2 antibody, Myozl2 antibody, C4orf5 antibody, CMH16 antibody, CS-1 antibody, myozenin 2 antibody, myozenin 2 S homeolog antibody, myozenin 2 L homeolog antibody, MYOZ2 antibody, myoz2.S antibody, myoz2.L antibody, myoz2 antibody, Myoz2 antibody

Background: MYOZ2 (Myozenin 2) is a Protein Coding gene. Diseases associated with MYOZ2 include Cardiomyopathy, Hypertrophic, 16 and Myoz2-Related Familial Hypertrophic Cardiomyopathy. GO annotations related to this gene include actin binding and telethonin binding. An important paralog of this gene is MYOZ1.The protein encoded by this gene belongs to a family of sarcomeric proteins that bind to calcineurin, a phosphatase involved in calcium-dependent signal transduction in diverse cell types. These family members tether calcineurin to alpha-actinin at the z-line of the sarcomere of cardiac and skeletal muscle cells, and thus they are important for calcineurin signaling. Mutations in this gene cause cardiomyopathy familial hypertrophic type 16, a hereditary heart disorder.

Molecular Weight:

Observed_MW: Refer to figures

Calculated_MW: 30 kDa

UniProt: Q9NPC6