MYO5A antibody

Catalog No. ABIN7264882

Product Details anti-MYO5A Antibody

Target: MYO5A (Myosin VA (MYO5A))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MYO5A antibody is un-conjugated

Application: Immunohistochemistry (IHC)

Characteristics: Polyclonal Antibody

Purification: Affinity purification

Immunogen: Recombinant fusion protein of human MYO5A (NP_000250.3).

Isotype: IgG

Application Details

Application Notes: IHC 1:50-1:100

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

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 MYO5A

Target: MYO5A (Myosin VA (MYO5A))

Alternative Name: MYO5A (MYO5A Products)

Synonyms: myo5a antibody, MGC53270 antibody, si:dkey-266j9.1 antibody, MYOA antibody, MYO5A antibody, D antibody, Dop antibody, Myh12 antibody, 9630007J19Rik antibody, AI413174 antibody, AI661011 antibody, Dbv antibody, MVa antibody, Myo5 antibody, MyoVA antibody, Sev-1 antibody, d antibody, d-120J antibody, flail antibody, flr antibody, DILUTE antibody, myoxin) antibody, non-muscle antibody, GS1 antibody, MYH12 antibody, MYO5 antibody, MYR12 antibody, myosin VA L homeolog antibody, myosin VAa antibody, myosin VA antibody, myosin va antibody, myo5a.L antibody, myo5aa antibody, MYO5A antibody, PY04789 antibody, Myo5a antibody

Background: This gene is one of three myosin V heavy-chain genes, belonging to the myosin gene superfamily. Myosin V is a class of actin-based motor proteins involved in cytoplasmic vesicle transport and anchorage, spindle-pole alignment and mRNA translocation. The protein encoded by this gene is abundant in melanocytes and nerve cells. Mutations in this gene cause Griscelli syndrome type-1 (GS1), Griscelli syndrome type-3 (GS3) and neuroectodermal melanolysosomal disease, or Elejalde disease. Multiple alternatively spliced transcript variants encoding different isoforms have been reported, but the full-length nature of some variants has not been determined.

Gene ID: 4644

UniProt: Q9Y4I1

Pathways: Hormone Transport, Peptide Hormone Metabolism