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Rabbit Anti-MYOM3/Cy5.5 Conjugated antibody
Rabbit Anti-MYOM3/Cy5.5 Conjugated antibody
MYOM3; MYOM3_HUMAN; Myomesin family member 3; Myomesin-3; RP11-293P20.1.
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  • NO.:SL19179R-Cy5.5
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted: Human,Mouse,Rat,Dog,Horse,)
    Applications:ICC IF
    concentration:1mg/ml
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Product Name Anti-MYOM3/Cy5.5
Chinese Name Cy5.5标记的肌间蛋白3抗体
Alias MYOM3; MYOM3_HUMAN; Myomesin family member 3; Myomesin-3; RP11-293P20.1.  
Research Area Tumour  Cell biology  immunology  Neurobiology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Mouse, Rat, Dog, Horse, )
Applications ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Molecular weight 162kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human MYOM3
Lsotype IgG
Purification affinity purified by Protein A
Storage Buffer 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
Product Detail background:
MYOM3 is a 1,437 amino acid protein that contains five fibronectin type-III domains and four Ig-like C2-type (immunoglobulin-like) domains. Existing as three alternatively spliced isoforms, the gene that encodes myomesin-3 maps to human chromosome 1p36.11 and mouse chromosome 4 D3. Chromosome 1 spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.

Subunit:
Homodimer.

Subcellular Location:
Cytoplasm, myofibril, sarcomere

Similarity:
Contains 5 fibronectin type-III domains.
Contains 4 Ig-like C2-type (immunoglobulin-like) domains.

Database links:

Entrez Gene: 127294 Human

SwissProt: Q5VTT5 Human

Unigene: 523413 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

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