Size: 200μL

Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.

Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.

Exp date: 12 months

Category ID_II: Primary Antibodies

Category ID_III: Polyclonal Antibodies

Abbreviation: MYO7A

Target Synonym: Deafness autosomal dominant 11;Deafness autosomal recessive 2;DFNA11;DFNB 2;DFNB2;Myo7a;Myosin 7a;Myosin VIIA (Usher syndrome 1B (autosomal recessive;severe));Myosin VIIa;Myosin;unconventional;family VII;member A;MYOVIIA;MYU7A;NSRD 2;NSRD2;Unconventional myosin VIIa;Ush 1B;Ush1b;Usher syndrome 1B

Research Areas: Cancer;Signal transduction

Conjugation: Unconjugated

Host: Rabbit

Species reactivity: Human;Mouse

Application: IHC

Isotype: IgG

Clonality: Polyclonal

Clone NO.:

UNIProt ID: Q13402

Accession:

Background: This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants.

Concentration: 0.6 mg/mL

Immunogen: Synthetic peptide of human MYO7A

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Purification method: Affinity purification

Dilution: IHC 1:50-1:200

Calculated MW:

ObservedMW: