Recombinant Human ALOX12B, GST-tagged
Cat.No. : | ALOX12B-9590H |
Product Overview : | Recombinant Human ALOX12B protein, fused to GST-tag, was expressed in E.coli and purified by GSH-sepharose. |
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- Gene Information
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Description : | This gene encodes an enzyme involved in the converstion of arachidonic acid to 12R-hydroxyeicosatetraenoic acid. Mutations in this gene are associated with nonbullous congenital ichthyosiform erythroderma. |
Source : | E.coli |
Species : | Human |
Tag : | GST |
Protein length : | 352-701a.a. |
Storage : | The protein is stored in PBS buffer at -20℃. Avoid repeated freezing and thawing cycles. |
Storage Buffer : | 1M PBS (58mM Na2HPO4,17mM NaH2PO4, 68mM NaCl, pH8. ) added with 100mM GSH and 1% Triton X-100,15%glycerol. |
Gene Name : | ALOX12B arachidonate 12-lipoxygenase, 12R type [ Homo sapiens ] |
Official Symbol : | ALOX12B |
Synonyms : | ALOX12B; arachidonate 12-lipoxygenase, 12R type; arachidonate 12-lipoxygenase, 12R-type; 12R LOX; 12R-lipoxygenase; epidermis-type lipoxygenase 12; 12R-LOX; |
Gene ID : | 242 |
mRNA Refseq : | NM_001139 |
Protein Refseq : | NP_001130 |
MIM : | 603741 |
UniProt ID : | O75342 |
Chromosome Location : | 17p13.1 |
Pathway : | Arachidonic acid metabolism, organism-specific biosystem; Arachidonic acid metabolism, conserved biosystem; IL23-mediated signaling events, organism-specific biosystem; Metabolic pathways, organism-specific biosystem; Serotonergic synapse, organism-specific biosystem; |
Function : | arachidonate 12-lipoxygenase activity; iron ion binding; lipoxygenase activity; metal ion binding; oxidoreductase activity; |
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ALOX12B-483H | Recombinant Human ALOX12B Protein, GST-tagged | +Inquiry |
◆ 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 (16)
Ask a questionMutations in the ALOX12B gene may lead to the development of cardiovascular disease, which can affect cardiovascular health.
The ALOX12B gene variant has not been shown to be associated with tumors.
There is no specific treatment for the ALOX12B gene mutation. Treatment is mostly based on symptom relief and reduction of disease progression.
A mutation of the ALOX12B gene can be diagnosed with a genetic test or blood test.
The regulatory mechanisms of ALOX12B gene include transcription factors, miRNA and other regulatory mechanisms.
Mutations in the ALOX12B gene may lead to the development of skin diseases that affect skin health.
ALOX12B gene mutation and liver disease has not been proven to have a clear link.
Current studies have shown that the ALOX12B variant is more common in Asian populations.
ALOX12B encodes the 12R-LOX enzyme, which is involved in biological processes such as lipid metabolism and inflammatory responses.
The polymorphism of ALOX12B gene can affect the activity of the enzyme it encodes, and thus affect related biological processes.
The SNP of ALOX12B gene has not been confirmed to have a clear association with drug metabolism.
The ALOX12B gene plays an important role in the body's inflammatory response and therefore may influence the function of the immune system.
Mutations in the ALOX12B gene have been linked to skin disorders, asthma, cardiovascular disease and more.
The ALOX12B gene can affect biological processes such as fat metabolism in the body, thus affecting body metabolism.
A mutant version of the ALOX12B gene has been linked to a rare inherited fat metabolism disorder called Allen's syndrome.
ALOX12B gene is more expressed in skin, liver, heart, kidney and other organs.
Customer Reviews (3)
Write a reviewALOX12B has good absorbability and high bioavailability.
Highly effective in signal transduction pathways.
Under different environmental conditions,ALOX12B showed good stability.
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