« Back
Home /
MYO7A Polyclonal Antibody

MYO7A Polyclonal Antibody

Item no.	E-AB-16626-120
Manufacturer	Elabscience
Amount	120 uL
Quantity options	120 uL 20 uL 200 uL 60 uL
Category	Oncology Neuroscience Neural Lineage Markers Antibodies By Cell Type Melanoma Cell Biology Cell Status Necrosis Cytoskeleton Immunohistochemistry ELISA Motor proteins Primary Antibodies Microglia Markers
Type	Antibody Polyclonal
Applications	IHC
Specific against	Human (Homo sapiens), Mouse (Murine, Mus musculus)
Host	Rabbit
Isotype	IgG
Conjugate/Tag	Unconjugated
ECLASS 10.1	32160702
ECLASS 11.0	32160702
UNSPSC	12352203
Alias	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
Similar products	member A, Myosin VIIa, Myo7a, DFNA11, DFNB2, MYOVIIA, MYU7A, NSRD2, severe)), Myosin, Deafness autosomal dominant 11, Deafness autosomal recessive 2, DFNB 2, Myosin 7a, NSRD 2, Ush 1B, Ush1b, Myosin VIIA (Usher syndrome 1B (autosomal recessive, unconventional, family VII, Unconventional myosin VIIa, Usher syndrome 1B
Shipping Condition	Cool pack
Hazard information	Comply with cargo safety certificate
Available
Manufacturer - Category	Primary Antibodies
Manufacturer - Targets	MYO7A
Shipping Temperature	The product is shipped with ice pack, upon receipt, store it immediately at the temperature recommended.
Storage Conditions	Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Manufacturer - Research Areas	Cancer, Signal transduction
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
Buffer	PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification Method	Affinity purification
Recommended Dilution	IHC 1:50-1:200
Santa Cruz #	sc-26709, sc-25834
Abbreviation	MYO7A
Clonality	Polyclonal
Immunogen	Synthetic peptide of human MYO7A
Category ID III	Polyclonal Antibodies

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.