MYO7A (Human) Recombinant Protein (Q01)
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More Files
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Specification
Product Description
Human MYO7A partial ORF ( NP_000251, 2118 a.a. - 2213 a.a.) recombinant protein with GST-tag at N-terminal.
Sequence
KQTTEPNFPEILLIAINKYGVSLIDPKTKDILTTHPFTKISNWSSGNTYFHITIGNLVRGSKLLCETSLGYKMDDLLTSYISQMLTAMSKQRGSRS
Host
Wheat Germ (in vitro)
Theoretical MW (kDa)
36.3
Interspecies Antigen Sequence
Mouse (98); Rat (97)
Preparation Method
Purification
Glutathione Sepharose 4 Fast Flow
Quality Control Testing
12.5% SDS-PAGE Stained with Coomassie Blue.
Storage Buffer
50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
Storage Instruction
Store at -80°C. Aliquot to avoid repeated freezing and thawing.
Note
Best use within three months from the date of receipt of this protein.
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Applications
Enzyme-linked Immunoabsorbent Assay
Western Blot (Recombinant protein)
Antibody Production
Protein Array
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Gene Info — MYO7A
Entrez GeneID
4647GeneBank Accession#
NM_000260Protein Accession#
NP_000251Gene Name
MYO7A
Gene Alias
DFNA11, DFNB2, MYOVIIA, MYU7A, NSRD2, USH1B
Gene Description
myosin VIIA
Gene Ontology
HyperlinkGene Summary
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. [provided by RefSeq
Other Designations
deafness, autosomal dominant 11|deafness, autosomal recessive 2|myosin VIIA (Usher syndrome 1B (autosomal recessive, severe))
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Interactome
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Disease
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