MYH3 anticorps (AA 30-80)

N° du produit ABIN5690063

Détail du produit anti-MYH3 anticorps

Antigène: MYH3 (Myosin Heavy Chain 3, Skeletal Muscle, Embryonic (MYH3))

Épitope: AA 30-80

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MYH3 est non-conjugé

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

Specificité: MYH3 antibody is human, mouse and rat reactive. MYH3 antibody is predicted to not cross-react with other members of the myosin heavy chain family.

Purification: MYH3 antibody is affinity chromatography purified via peptide column.

Immunogène: MYH3 antibody was raised against a 19 amino acid peptide near the amino terminus of human MYH3.

The immunogen is located within amino acids 30 - 80 of MYH3.

Isotype: IgG

Information d'application

Indications d'application: MYH3 antibody can be used for detection of MYH3 by Western blot at 1 μ,g/mL. Antibody can also be used for immunohistochemistry starting at 5 μ,g/mL.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: MYH3 antibody is supplied in PBS containing 0.02 % sodium azide.

Agent conservateur: Sodium azide

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

Stock: 4 °C,-20 °C

Stockage commentaire: MYH3 antibody can be stored at 4°C for three months and -20°C, stable for up to one year.

Détails sur MYH3

Antigène: MYH3 (Myosin Heavy Chain 3, Skeletal Muscle, Embryonic (MYH3))

Autre désignation: MYH3 (MYH3 Produits)

Sujet: Myosins are actin-based motor proteins that function in the generation of mechanical force in eukaryotic cells (1). MYH3 (myosin, heavy chain, skeletal muscle, embryonic) plays a significant role in skeletal muscle development (2) and is also essential for the proper morphology and function of the developing heart (3). Mutations in this gene have been associated with Freeman-Sheldon syndrome and Sheldon-Hall syndrome (4).

Poids moléculaire: Predicted: 240 kDa

Observed: 245 kDa

ID gène: 4621

NCBI Accession: NP_002461

UniProt: P11055