MYH10 antibody (AA 1150-1450)

Catalog No. ABIN7116635

The Rabbit Polyclonal anti-MYH10 antibody has been validated for WB, IHC and ELISA. It is suitable to detect MYH10 in samples from Human, Mouse and Rat.

Quick Overview for MYH10 antibody (AA 1150-1450) (ABIN7116635)

Target: MYH10 (Myosin, Heavy Polypeptide 10, Non-Muscle (MYH10))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MYH10 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA

Product Details anti-MYH10 Antibody

Binding Specificity: AA 1150-1450

Purpose: MYH10 antibody

Purification: Immunogen affinity purified

Purity: ≥95 % as determined by SDS-PAGE

Immunogen:

Immunogen sequence: 1150-1450aa

Immunogen: myosin, heavy chain 10, non-muscle

Isotype: IgG

Application Details

Application Notes: WB: 1:500 - 1:2000, IHC: 1:50 - 1:200

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide and 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.

Handling Advice: Avoid repeated freeze / thaw cycles.

Storage: -20 °C

Storage Comment: -20°C for 12 months

Expiry Date: 12 months

Target Details for MYH10

Target: MYH10 (Myosin, Heavy Polypeptide 10, Non-Muscle (MYH10))

Alternative Name: MYH10

Background:

Synonyms: Myosin-10|Cellular myosin heavy chain, type B|Myosin heavy chain 10|Myosin heavy chain, non-muscle IIb|Non-muscle myosin heavy chain B (NMMHC-B)|Non-muscle myosin heavy chain IIb (NMMHC II-b, NMMHC-IIB)|MYH10

Background: This gene encodes a member of the myosin superfamily. The protein represents a conventional non-muscle myosin, it should not be confused with the unconventional myosin-10 (MYO10). Myosins are actin-dependent motor proteins with diverse functions including regulation of cytokinesis, cell motility, and cell polarity. Mutations in this gene have been associated with May-Hegglin anomaly and developmental defects in brain and heart. Multiple transcript variants encoding different isoforms have been found for this gene.

Molecular Weight: 250 kDa

Gene ID: 4628

UniProt: P35580