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Anti-EEPD1 Polyclonal Antibody is a Rabbit antibody targeting EEPD1. Anti-EEPD1 Polyclonal Antibody can be used in WB.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 50 μL | $222 | 7-10 days | 7-10 days | |
| 100 μL | $374 | 7-10 days | 7-10 days | |
| 200 μL | $527 | 7-10 days | 7-10 days |
| Description | Anti-EEPD1 Polyclonal Antibody is a Rabbit antibody targeting EEPD1. Anti-EEPD1 Polyclonal Antibody can be used in WB. |
| Ig Type | IgG |
| Reactivity | Mouse (predicted:Human,Rat,Dog,Pig,Cow,Horse,Rabbit,Sheep) |
| Application | |
| Recommended Dose | WB: 1:500-2000 |
| Antibody Type | Polyclonal |
| Host Species | Rabbit |
| Construction | Polyclonal Antibody |
| Purification | Protein A purified |
| Appearance | Liquid |
| Formulation | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
| Concentration | 1mg/ml |
| Research Background | 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. |
| Immunogen | KLH conjugated synthetic peptide: human EEPD1 |
| Antigen Species | Human |
| Gene Name | EEPD1 |
| Gene ID | |
| Protein Name | Endonuclease/exonuclease/phosphatase family domain-containing protein 1 |
| Uniprot ID |
| Molecular Weight | Theoretical: 62 kDa. |
| Stability & Storage | Store at 2°C-8°C for 1 month. Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles. |
| Transport | Shipping with blue ice. |
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