Myosin 9 antibody (C-Term)

Catalog No. ABIN7464469

The Mouse Monoclonal anti-Myosin 9 antibody has been validated for WB and IHC (p). It is suitable to detect Myosin 9 in samples from Human.

Quick Overview for Myosin 9 antibody (C-Term) (ABIN7464469)

Target: Myosin 9 (MYH9)

Reactivity: Human

Host: Mouse

Clonality: Monoclonal

Conjugate: This Myosin 9 antibody is un-conjugated

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

Clone: GT566

Product Details anti-Myosin 9 Antibody

Binding Specificity: C-Term

Cross-Reactivity: Human, Mouse

Purification: Affinity purified by Protein A.

Immunogen: Carrier-protein conjugated synthetic peptide encompassing a sequence within the C-terminus region of human MYH9. The exact sequence is proprietary.

Isotype: IgG2b

Application Details

Application Notes: WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: HeLa , MYH9-transfected 293T , Neuro2A , C8D30 , NIH-3T3 , Raw264.7 , C2C12

Validation: Overexpression

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, No Preservative

Preservative: Without preservative

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for Myosin 9

Target: Myosin 9 (MYH9)

Alternative Name: myosin heavy chain 9

Background: Myosin heavy chain 9 , BDPLT6 , DFNA17 , EPSTS , FTNS , MATINS , MHA , NMHC-II-A , NMMHC-IIA , NMMHCA,This gene encodes a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain. The protein is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in MYH9 are the cause of non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness. [provided by RefSeq]

Molecular Weight: 227 kDa

Gene ID: 4627

UniProt: P35579

Pathways: Regulation of G-Protein Coupled Receptor Protein Signaling, Integrin Complex