Recombinant Human Blood Pressure QTL
Cat.No. : | BP1-83H |
Product Overview : | Recombinant Human Blood pressure QTL protein 103-168 a.a. expressed inE.coli,35 kDa. |
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Cat. No. : | BP1-83H |
Description : | BP-1 gene, a member of the DLX homeobox gene family, is overexpressed in 80% of breast cancer patients, and thus represents a potential new target for diagnosis and treatment. |
Source : | Escherichia Coli. |
Presentation : | 5µg/50µl Recombinant Human BP-1 protein at 100µg/ml in 50mM Tris-Acetate, pH7.5, 1mM EDTA and 20% Glycerol. |
Applications : | •ELISA•Inhibition Assays•Western Blotting. |
Characterization : | On SDS-PAGE commassie blue stained gel, the purified recombinant protein shows a band at 35 kDa. |
Activity : | Not known. |
Storage : | Store vial at -20°Cto -80°C. When stored at the recommended temperature, this protein is stable for 12 months. |
Tag : | Non |
Protein length : | 103-168 |
Gene Name : | BP1 Blood pressure QTL 1 [ Homo sapiens ] |
Synonyms : | BP1; Blood pressure QTL 1; Blood pressure QTL 1 (human) |
Gene ID : | 474256 |
Gene Name : | BP1 Blood pressure QTL 1 [ Homo sapiens ] |
Synonyms : | BP1; Blood pressure QTL 1; Blood pressure QTL 1 (human) |
Gene ID : | 474256 |
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Not For Human Consumption!
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Customer Reviews (3)
Write a reviewThe structure of BP1 was verified with no abnormal protein folding or inactivation.
The production process of BP1 products is environmentally friendly and sustainable, in line with the concept of green production.
When using BP1 for experiments, it is easy to operate and does not require complex operating steps.
Q&As (6)
Ask a questionYes, mutations in the BP1 gene can be hereditary diseases that follow a certain pattern of inheritance.
BP1 gene mutation can be detected by gene sequencing, PCR and other technologies.
The treatment for BP1 gene mutation includes drug therapy, lifestyle intervention, gene therapy, etc., and the specific method should be determined according to the patient's condition.
Mutations in the BP1 gene may affect the prognosis of patients, including disease progression and treatment response.
Mutations in the BP1 gene may lead to changes in gene expression, which in turn affect the structure and function of the relevant protein.
The frequency of BP1 mutations in the population varies according to the type of mutation and ethnic differences.
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