MYO7A Polyclonal Antibody
| Code | Size | Price |
|---|
| E-AB-16626-20uL | 20uL | £125.00 |
Quantity:
| E-AB-16626-60uL | 60uL | £172.00 |
Quantity:
| E-AB-16626-120uL | 120uL | £237.00 |
Quantity:
| E-AB-16626-200uL | 200uL | £344.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Host Type: Rabbit
Antibody Isotype: IgG
Antibody Clonality: Polyclonal
Regulatory Status: RUO
Target Species:
- Human
- Mouse
Applications:
- Enzyme-Linked Immunosorbent Assay (ELISA)
- Immunohistochemistry (IHC)
Shipping:
Ice packs
Storage:
-20°C
Further Information
Abbreviation:
MYO7A
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.
Buffer:
PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Concentration:
0.6 mg/mL
Conjugation:
Unconjugated
Dilution:
IHC 1:50-1:200
Immunogen:
Synthetic peptide of human MYO7A
Purification method:
Affinity purification
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
UNIProt ID:
Q13402