ARG64475
anti-EXO1 antibody
anti-EXO1 antibody for Western blot and Human
Gene Regulation antibody
Overview
Product Description | Goat Polyclonal antibody recognizes EXO1 |
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Tested Reactivity | Hu |
Tested Application | WB |
Specificity | This antibody is expected to recognise all three reported isoforms (NP_003677.3; NP_006018.3 and NP_569082.1) |
Host | Goat |
Clonality | Polyclonal |
Isotype | IgG |
Target Name | EXO1 |
Antigen Species | Human |
Immunogen | C-HRNYSPRPESGT |
Conjugation | Un-conjugated |
Alternate Names | Exonuclease I; hExoI; EC 3.1.-.-; hExo1; HEX1; Exonuclease 1 |
Application Instructions
Application Suggestion |
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Application Note | WB: Recommend incubate at RT for 1h. * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. |
Properties
Form | Liquid |
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Purification | Purified from goat serum by antigen affinity chromatography. |
Buffer | Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA. |
Preservative | 0.02% Sodium azide |
Stabilizer | 0.5% BSA |
Concentration | 0.5 mg/ml |
Storage Instruction | For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. |
Note | For laboratory research only, not for drug, diagnostic or other use. |
Bioinformation
Database Links | |
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Background | This gene encodes a protein with 5' to 3' exonuclease activity as well as an RNase H activity. It is similar to the Saccharomyces cerevisiae protein Exo1 which interacts with Msh2 and which is involved in mismatch repair and recombination. Alternative splicing of this gene results in three transcript variants encoding two different isoforms. [provided by RefSeq, Jul 2008] |
Research Area | Gene Regulation antibody |
Calculated MW | 94 kDa |
PTM | Phosphorylated upon DNA damage and in response to agents stalling DNA replication, probably by ATM or ATR. Phosphorylation at Ser-454, Thr-621 and Ser-714 is induced upon DNA-damage caused by treatment with hydroxyurea (HU) but not upon IR treatment. The HU-induced EXO1 triple phosphorylation facilitates destabilisation/degradation of the protein. |