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MYO7A Polyclonal Antibody

Cat:E-AB-13433
Manual MSDS

Price: $ 399

Price: $ 240

Price: $ 143

Price: $ 73

Size:
200μL 120μL 60μL 20μL
Quantity:
  • Host: Rabbit
  • Reactivity: Human;Mouse
  • Applications: IHC
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Product Details
Verified Samples Verified Samples in IHC:Human thyroid cancer,Human brain
Dilution

IHC 1:25-1:100

Western Blot Operation Guide
Clonality Polyclonal
Immunogen Synthetic peptide of human MYO7A
Abbre MYO7A
Synonyms 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
Swissprot
Cellular Localization Cytoplasmic, cytoskeleton
Concentration 0.5 mg/mL
Buffer PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification Method Affinity purification
Research Areas Cancer; Signal Transduction
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping Biological ice pack at 4 ℃
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.