METAP1 Antibody
Mouse Monoclonal Antibody (Mab)
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Application 
  | WB, E | 
|---|---|
| Primary Accession | P53582 | 
| Other Accession | NP_055958.2 | 
| Reactivity | Human | 
| Host | Mouse | 
| Clonality | Monoclonal | 
| Isotype | IgG1,k | 
| Clone Names | 248CT14.6.1 | 
| Calculated MW | 43215 Da | 
| Gene ID | 23173 | 
|---|---|
| Other Names | Methionine aminopeptidase 1 {ECO:0000255|HAMAP-Rule:MF_03174}, MAP 1 {ECO:0000255|HAMAP-Rule:MF_03174}, MetAP 1 {ECO:0000255|HAMAP-Rule:MF_03174}, 341118 {ECO:0000255|HAMAP-Rule:MF_03174}, Peptidase M 1 {ECO:0000255|HAMAP-Rule:MF_03174}, METAP1, KIAA0094 | 
| Target/Specificity | This METAP1 monoclonal antibody is generated from mouse immunized with METAP1 recombinant protein. | 
| Dilution | WB~~1:2000 E~~Use at an assay dependent concentration.  | 
| Format | Purified monoclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein G column, followed by dialysis against PBS. | 
| Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. | 
| Precautions | METAP1 Antibody is for research use only and not for use in diagnostic or therapeutic procedures. | 
| Name | METAP1 | 
|---|---|
| Synonyms | KIAA0094 | 
| Function | Cotranslationally removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met- Ala-, Cys, Gly, Pro, Ser, Thr, or Val). Required for normal progression through the cell cycle. | 
| Cellular Location | Cytoplasm {ECO:0000255|HAMAP-Rule:MF_03174}. | 
For Research Use Only. Not For Use In Diagnostic Procedures.
Provided below are standard protocols that you may find useful for product applications.
BACKGROUND
METAP1 removes the amino-terminal methionine from nascent proteins. Required for normal progression through the cell cycle.
REFERENCES
Xiao, Q., et al. Biochemistry 49(26):5588-5599(2010)
Rose, J.E., et al. Mol. Med. 16 (7-8), 247-253 (2010) :
Ross, C.J., et al. Nat. Genet. 41(12):1345-1349(2009)
Hu, X.V., et al. Biochemistry 46(44):12833-12843(2007)
Ewing, R.M., et al. Mol. Syst. Biol. 3, 89 (2007) :
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