Recombinant Mouse Cbr1 Protein, MYC/DDK-tagged
Cat.No. : | Cbr1-791M |
Product Overview : | Purified recombinant protein of full-length mouse carbonyl reductase 1 (Cbr1), with C-terminal MYC/DDK tag, expressed in HEK293T cells. |
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Description : | Ubiquitous expression in kidney adult (RPKM 160.7), duodenum adult (RPKM 131.5) and 28 other tissues. |
Source : | HEK293T |
Species : | Mouse |
Tag : | Myc&DDK |
Molecular Mass : | 30.6 kDa |
Purity : | >80% as determined by SDS-PAGE and Coomassie blue staining |
Stability : | Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles. |
Storage : | Store at -80 centigrade after receiving vials. |
Concentration : | >50 μg/mL as determined by microplate BCA method |
Storage Buffer : | 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol. |
Gene Name : | Cbr1 carbonyl reductase 1 [ Mus musculus (house mouse) ] |
Official Symbol : | Cbr1 |
Synonyms : | Cbr1; carbonyl reductase 1; CR; Cbr; PG-9-KR; AW261796; carbonyl reductase [NADPH] 1; 15-hydroxyprostaglandin dehydrogenase; 20-beta-hydroxysteroid dehydrogenase; Carbonyl reductase [NADPH] 1 (NADPH-dependent carbonyl reductase 1); NADPH-dependent carbonyl reductase 1; prostaglandin 9-ketoreductase; prostaglandin-E(2) 9-reductase; EC 1.1.1.141; EC 1.1.1.184; EC 1.1.1.189; EC 1.1.1.197; EC 1.1.1.53 |
Gene ID : | 12408 |
mRNA Refseq : | NM_007620 |
Protein Refseq : | NP_031646 |
UniProt ID : | P48758 |
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◆ Lysates | ||
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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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Q&As (6)
Ask a questionGene knockout or knockdown techniques can be used to study the function and mechanism of action of CBR1 proteins. By knocking out or knocking down CBR genes, changes in processes such as cholesterol metabolism and fatty acid synthesis can be observed to further understand their functions and mechanisms of action.
Immunohistochemistry and other methods can be used to analyze the effect of phosphorylation modification of CBR1 protein on its function. Studies have shown that phosphorylation modification can affect the activity and expression level of CBR1 protein, which in turn affects processes such as cholesterol metabolism and fatty acid synthesis.
Yeast two-hybridization, co-immunoprecipitation and other methods can be used to study the interaction of CBR1 protein with other proteins. These methods can determine the types and sites of interacting proteins, and further reveal the regulatory mechanism of CBR1 protein in cells.
The metabolic pathway of CBR1 protein can be analyzed using isotope labeling techniques. The labeled isotope is introduced into the cell or tissue.
It can provide a reference for clinical practice and guide the diagnosis, treatment and prevention of CBR1 protein by detecting the expression level of CBR1 protein and understanding its mechanism of action.
The expression level of CBR1 protein can be regulated through drug interventions, such as the use of cholesterol synthesis inhibitors, fatty acid synthesis inhibitors, etc. These drugs can inhibit the activity or expression level of CBR1 protein, thus achieving the purpose of treating diseases.
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