Recombinant Full Length Human ALOX12B Protein, GST-tagged
Cat.No. : | ALOX12B-1467HF |
Product Overview : | Human ALOX12B full-length ORF ( NP_001130.1, 1 a.a. - 701 a.a.) recombinant protein with GST-tag at N-terminal. |
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Description : | This gene encodes an enzyme involved in the conversion of arachidonic acid to 12R-hydroxyeicosatetraenoic acid. Mutations in this gene are associated with nonbullous congenital ichthyosiform erythroderma. [provided by RefSeq, Sep 2015] |
Source : | In Vitro Cell Free System |
Species : | Human |
Tag : | GST |
Molecular Mass : | 106.8 kDa |
Protein Length : | 701 amino acids |
AA Sequence : | MATYKVRVAT GTDLLSGTRD SISLTIVGTQ GESHKQLLNH FGRDFATGAV GQYTVQCPQD LGELIIIRLH KERYAFFPKD PWYCNYVQIC APNGRIYHFP AYQWMDGYET LALREATGKT TADDSLPVLL EHRKEEIRAK QDFYHWRVFL PGLPSYVHIP SYRPPVRRHR NPNRPEWNGY IPGFPILINF KATKFLNLNL RYSFLKTASF FVRLGPMALA FKVRGLLDCK HSWKRLKDIR KIFPGKKSVV SEYVAEHWAE DTFFGYQYLN GVNPGLIRRC TRIPDKFPVT DDMVAPFLGE GTCLQAELEK GNIYLADYRI MEGIPTVELS GRKQHHCAPL CLLHFGPEGK MMPIAIQLSQ TPGPDCPIFL PSDSEWDWLL AKTWVRYAEF YSHEAIAHLL ETHLIAEAFC LALLRNLPMC HPLYKLLIPH TRYTVQINSI GRAVLLNEGG LSAKGMSLGV EGFAGVMVRA LSELTYDSLY LPNDFVERGV QDLPGYYYRD DSLAVWNALE KYVTEIITYY YPSDAAVEGD PELQSWVQEI FKECLLGRES SGFPRCLRTV PELIRYVTIV IYTCSAKHAA VNTGQMEFTA WMPNFPASMR NPPIQTKGLT TLETFMDTLP DVKTTCITLL VLWTLSREPD DRRPLGHFPD IHFVEEAPRR SIEAFRQRLN QISHDIRQRN KCLPIPYYYL DPVLIENSIS I |
Applications : | Enzyme-linked Immunoabsorbent Assay; Western Blot (Recombinant protein); Antibody Production; Protein Array |
Storage : | Store at -80 centigrade. Aliquot to avoid repeated freezing and thawing. |
Storage Buffer : | 50 mM Tris-HCl, 10 mM reduced Glutathione, pH=8.0 in the elution buffer. |
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 |
Products Types
◆ Recombinant Protein | ||
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ALOX12B-483H | Recombinant Human ALOX12B Protein, GST-tagged | +Inquiry |
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◆ Lysates | ||
ALOX12B-8898HCL | Recombinant Human ALOX12B 293 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 (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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