Recombinant Human DUSP14, His & MBP tagged
Cat.No. : | DUSP14-2511H |
Product Overview : | Recombinant Human DUSP14 (O95147) (Met 1 –His 191), fused with an N-terminal polyhistidine-tagged MBP tag, was produced in E. coli. |
- Specification
- Gene Information
- Related Products
Source : | E.coli |
Species : | Human |
Tag : | His & MBP |
Form : | Lyophilized from sterile 50 mM Tris, pH 8.0. Normally 5 % - 8 % trehalose, mannitol and 0.01% Tween80 are added as protectants before lyophilization. |
Molecular Mass : | The recombinant human DUSP14/MBP fusion protein consists of 587 amino acids and has a calculated molecular mass of 65 kDa. It migrates as an approximately 60 kDa band in SDS-PAGE under reducing conditions. |
Protein Length : | Met 1 –His 191 |
Purity : | > 88 % as determined by SDS-PAGE |
Storage : | Samples are stable for up to twelve months from date of receipt at -20°C to -80°C Store it under sterile conditions at -20°C to -80°C. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles. |
Reconstitution : | It is recommended that sterile water be added to the vial to prepare a stock solution of 0.2 ug/ul. Centrifuge the vial at 4℃ before opening to recover the entire contents. |
Gene Name : | DUSP14 dual specificity phosphatase 14 [ Homo sapiens ] |
Official Symbol : | DUSP14 |
Synonyms : | DUSP14; dual specificity phosphatase 14; dual specificity protein phosphatase 14; MKP 1 like protein tyrosine phosphatase; MKP L; MKP6; MKP-6; MAP kinase phosphatase 6; MKP-1 like protein tyrosine phosphatase; MKP-1-like protein tyrosine phosphatase; mitogen-activated protein kinase phosphatase 6; MKP-L; |
Gene ID : | 11072 |
mRNA Refseq : | NM_007026 |
Protein Refseq : | NP_008957 |
MIM : | 606618 |
UniProt ID : | O95147 |
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◆ Lysates | ||
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Related Gene
For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
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