Recombinant Rat Cbr1 Protein, His-tagged
Cat.No. : | Cbr1-593R |
Product Overview : | Recombinant Rat Cbr1(Ser2~Asp271) fused with His tag at N-terminal was expressed in E. coli. |
- Specification
- Gene Information
- Related Products
Source : | E. coli |
Species : | Rat |
Tag : | His |
Form : | PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300. |
Molecular Mass : | 33.4kDa |
Protein length : | Ser2~Asp271 |
Endotoxin : | <1.0EU per 1ug (determined by the LAL method) |
Purity : | > 95% |
Applications : | Positive Control; Immunogen; SDS-PAGE; WB. If bio-activity of the protein is needed, please check active protein |
Stability : | The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37 centigrade for 48h, and no obvious degradation and precipitation were observed. The loss rate is less than 5% within the expiration date under appropriate storage condition. |
Storage : | Avoid repeated freeze/thaw cycles. Store at 2-8 centigrade for one month. Aliquot and store at -80 centigrade for 12 months. |
Reconstitution : | Reconstitute in PBS or others |
Gene Name : | Cbr1 carbonyl reductase 1 [ Rattus norvegicus ] |
Official Symbol : | Cbr1 |
Synonyms : | CBR1; carbonyl reductase 1; carbonyl reductase [NADPH] 1; Cbr 1; prostaglandin 9-ketoreductase; prostaglandin-E(2) 9-reductase; 20-beta-hydroxysteroid dehydrogenase; NADPH-dependent carbonyl reductase 1; 15-hydroxyprostaglandin dehydrogenase; Cbr; MGC124927; |
Gene ID : | 29224 |
mRNA Refseq : | NM_019170 |
Protein Refseq : | NP_062043 |
UniProt ID : | P47727 |
Products Types
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CBR1-591H | Recombinant Human CBR1 Protein, His-tagged | +Inquiry |
CBR1-1351H | Recombinant Human CBR1 Protein (2-277 aa), His-tagged | +Inquiry |
◆ Lysates | ||
CBR1-288HCL | Recombinant Human CBR1 cell lysate | +Inquiry |
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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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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