Elabscience

MYO7A Polyclonal Antibody

Product Code:
 
E-AB-16626
Product Group:
 
Primary Antibodies
Supplier:
 
Elabscience
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
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Immunohistochemistry of paraffin-embedded Human prostate cancer tissue using MYO7A Polyclonal Antibody at dilution 1:30
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Immunohistochemistry of paraffin-embedded Human brain tissue using MYO7A Polyclonal Antibody at dilution 1:30
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Immunohistochemistry of paraffin-embedded Human prostate cancer tissue using MYO7A Polyclonal Antibody at dilution 1:30
Immunohistochemistry of paraffin-embedded Human brain tissue using MYO7A Polyclonal Antibody at dilution 1:30

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E-AB-16626-20uL20uL£125.00
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E-AB-16626-60uL60uL£172.00
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E-AB-16626-120uL120uL£237.00
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E-AB-16626-200uL200uL£344.00
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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

Documents