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Rabbit Anti-CCDC87 antibody
Rabbit Anti-CCDC87 antibody
CCD87_HUMAN; Ccdc87; coiled coil domain containing 87; coiled coil domain containing protein 87; Coiled-coil domain-containing protein 87; FLJ10786.
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  • NO.:SL8140R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Human,(predicted: Mouse,Rat,)
    Applications:WB ELISA IHC-P IHC-F IF
    concentration:1mg/ml
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Details

Product Name CCDC87
Chinese Name 卷曲螺旋结构域蛋白87抗体
Alias CCD87_HUMAN; Ccdc87; coiled coil domain containing 87; coiled coil domain containing protein 87; Coiled-coil domain-containing protein 87; FLJ10786.  
Research Area Cell biology  immunology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Human,  (predicted: Mouse, Rat, )
Applications WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 96kDa
Cellular localization The nucleus cytoplasmic 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human CCDC87: 65-170/849 
Lsotype IgG
Purification affinity purified by Protein A
Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
Product Detail CCDC87 is an 849 amino acid protein encoded by a gene that maps to human chromosome 11q13.2. Chromosome 11, which comprises approximately 4% of the human genome, is considered a gene and disease association-dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations, while Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11-encoded genes

SWISS:
Q9NVE4

Gene ID:
55231

Database links:

Entrez Gene: 55231 Human

SwissProt: Q9NVE4 Human

Unigene: 121072 Human



Product Picture
Sample: MCF-7 (Human)cell Lysate at 40 ug
Primary: Anti-CCDC87(SL8140R)at 1/300 dilution
Secondary: IRDye800CW Goat Anti-RabbitIgG at 1/20000 dilution
Predicted band size: 96kD
Observed band size: 100kD

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