MYO7A Polyclonal Antibody

CAT: 0866-RD76975A-01Size: 20 µLDry Ice: NoHazardous: No
CAT#:0866-RD76975A-01Size:20 µL
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AVAILABILITY: InStock
24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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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.
Description
This is a MYO7A Polyclonal Antibody from Reddot Biotech. This product is for Research Use Only.
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
Swiss Prot
Q13402
Accession Number
NP_000251
Reactivity
Human, Mouse
Immunogen
Synthetic peptide of human MYO7A
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Polyclonal Antibody
Applications
IHC, ELISA
Purification Method
Affinity purification
Assay Type
Antibody
Concentration
0.5 mg/mL
Dilution
IHC 1:25-1:100
Buffer
PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Storage Conditions
Store at -20°C. Avoid freeze / thaw cycles.
Host or Source
Rabbit
Isotype
IgG

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