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Rabbit Anti-CCDC38 antibody
Rabbit Anti-CCDC38 antibody
CCDC38 coiled coil domain containing 38; Coiled coil domain containing 38; FLJ40089; CCD38_HUMAN.
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  • NO.:SL8130R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted: Human,Mouse,Rat,Chicken,Dog,Pig,Cow,Horse,Rabbit,)
    Applications:WB IHC-P IHC-F IF
    concentration:1mg/ml
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Product Name CCDC38
Chinese Name 卷曲螺旋结构域蛋白38抗体
Alias CCDC38 coiled coil domain containing 38; Coiled coil domain containing 38; FLJ40089; CCD38_HUMAN.  
Research Area Cell biology  immunology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Rabbit, )
Applications WB=1:500-2000 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 65kDa
Cellular localization The nucleus cytoplasmic 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human CCDC38: 451-563/563 
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. CCDC38 (coiled-coil domain containing 38) is a 563 amino acid protein encoded by a gene that maps to human chromosome 12q23.1. Encoding over 1,100 genes, chromosome 12 comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.

SWISS:
Q502W7

Gene ID:
120935

Database links:

Entrez Gene: 120935 Human

Entrez Gene: 237465 Mouse

SwissProt: Q502W7 Human

SwissProt: Q8CDN8 Mouse

Unigene: 210377 Human

Unigene: 477086 Mouse



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