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Antibodies

MYO7A Polyclonal Antibody

Product Sizes
20 ul
£148.00
RD79162A-20UL
60 ul
£242.00
RD79162A-60UL
120 ul
£372.00
RD79162A-120UL
200 ul
£585.00
RD79162A-200UL
About this Product
SKU:
RD79162A
Additional Names:
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
Application:
ELISA, Immunohistochemistry
Buffer:
PBS
Clonality:
Polyclonal
Concentration:
0.6 mg/ml
Extra Details:
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.|This is a MYO7A Polyclonal Antibody from Reddot Biotech. This product is for Research Use Only.
Host:
Rabbit
Immunogen:
Synthetic peptide of human MYO7A
Isotype:
IgG
Purification:
Affinity Purified
Reactivities:
Human, Mouse
Shipping Conditions:
Blue Ice
Storage Conditions:
-20[o]C Avoid freeze/thaw cycles.
Supplier:
Reddot
Type:
Antibody: Polyclonal Antibody