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Rabbit Anti-CCDC83 antibody
Rabbit Anti-CCDC83 antibody
Coiled coil domain containing 83; Coiled coil domain containing protein 83; HSD9; QtsA 10152; QtsA 19320; CCD83_HUMAN.
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  • NO.:SL8087R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted: Human,Mouse,Rat,Dog,Pig,Cow,Rabbit,Sheep,)
    Applications:ELISA IHC-P IHC-F IF
    concentration:1mg/ml
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Product Name CCDC83
Chinese Name 卷曲螺旋结构域蛋白83抗体
Alias Coiled coil domain containing 83; Coiled coil domain containing protein 83; HSD9; QtsA 10152; QtsA 19320; CCD83_HUMAN.  
Research Area Cardiovascular  Cell biology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Rabbit, Sheep, )
Applications 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 49kDa
Cellular localization The nucleus cytoplasmic The cell membrane 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human CCDC83: 101-200/413 
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 The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion, and drug extrusion and delivery. CCDC83 (coiled-coil domain-containing protein 83), also known as HSD9, is 413 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding CCDC83 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.

SWISS:
Q8IWF9

Gene ID:
220047

Database links:

Entrez Gene: 220047 Human

Entrez Gene: 617342 Cow

SwissProt: Q2TA00 Cow

SwissProt: Q8IWF9 Human

Unigene: 567774 Human



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