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Rabbit Anti-EEPD1 antibody
Rabbit Anti-EEPD1 antibody
EEPD1; EEPD1_HUMAN; Endonuclease/exonuclease/phosphatase family domain containing 1; Endonuclease/exonuclease/phosphatase family domain-containing protein 1; HSPC107; KIAA1706; OTTHUMP00000206928.
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  • NO.:SL14506R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Mouse,(predicted: Human,Rat,Dog,Pig,Cow,Horse,Rabbit,Sheep,)
    Applications:WB ELISA
    concentration:1mg/ml
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Details

Product Name EEPD1
Chinese Name EEPD1蛋白抗体
Alias EEPD1; EEPD1_HUMAN; Endonuclease/exonuclease/phosphatase family domain containing 1; Endonuclease/exonuclease/phosphatase family domain-containing protein 1; HSPC107; KIAA1706; OTTHUMP00000206928.  
Research Area Cell biology  Neurobiology  Epigenetics  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Mouse,  (predicted: Human, Rat, Dog, Pig, Cow, Horse, Rabbit, Sheep, )
Applications WB=1:500-2000 ELISA=1:5000-10000 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 62kDa
Cellular localization The nucleus 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human EEPD1: 9-100/569 
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 EEPD1 is a 569 amino acid protein that contains one HhH domain. A significant decrease in the relative transcriptional level of EEPD1 is induced by long-term heat stress exposure. Conversely, EEPD1 is up-regulated in bovine adipogenic processes related to intramuscular preadipocyte differentiation. Encoded by a gene that maps to human chromosome 7p14.2, EEPD1 plays a role in DNA binding and repair. Chromosome 7 makes up about 5% of the human genome and contains 158 million bases encoding more than 1,000 genes. Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome are associated with Chromosome 7.

Similarity:
Contains 1 HhH domain.

SWISS:
Q7L9B9

Gene ID:
80820

Database links:

Entrez Gene: 80820 Human

Entrez Gene: 315500 Rat

SwissProt: Q7L9B9 Human

SwissProt: Q5XI74 Rat

Unigene: 487994 Human

Unigene: 110716 Rat



Product Picture
Sample: Small intestine (Mouse) Lysate at 40 ug
Primary: Anti-EEPD1 (SL14506R) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 62 kD
Observed band size: 60 kD
Sample: Liver (Mouse) Lysate at 40 ug
Primary: Anti-EEPD1 (SL14506R) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 62 kD
Observed band size: 60 kD

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