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Image Unavailable-10369-352

Anti-ALOX5 Rabbit Polyclonal Antibody

Catalog Number: (10369-352)
Supplier: Bioss
Description: This gene encodes a member of the lipoxygenase gene family and plays a dual role in the synthesis of leukotrienes from arachidonic acid. The encoded protein, which is expressed specifically in bone marrow-derived cells, catalyzes the conversion of arachidonic acid to 5(S)-hydroperoxy-6-trans-8,11,14-cis-eicosatetraenoic acid, and further to the allylic epoxide 5(S)-trans-7,9-trans-11,14-cis-eicosatetrenoic acid (leukotriene A4). Leukotrienes are important mediators of a number of inflammatory and allergic conditions. Mutations in the promoter region of this gene lead to a diminished response to antileukotriene drugs used in the treatment of asthma and may also be associated with atherosclerosis and several cancers. Alternatively spliced transcript variants have been observed, but their full-length nature has not been determined.
Image Unavailable-CAPIPA5-18567

Anti-ALOX5 Goat Polyclonal Antibody

Catalog Number: (CAPIPA5-18567)
Supplier: Thermo Scientific
Description: This antibody is predicted to react with canine and mouse based on sequence homology. This gene encodes a member of the lipoxygenase gene family and plays a dual role in the synthesis of leukotrienes from arachidonic acid. The encoded protein, which is expressed specifically in bone marrow-derived cells, catalyzes the conversion of arachidonic acid to 5-hydroperoxy-6-trans-8,11,14-cis-eicosatetraenoic acid, and further to the allylic epoxide 5-trans-7,9-trans-11,14-cis-eicosatetrenoic acid . Leukotrienes are important mediators of a number of inflammatory and allergic conditions. Mutations in the promoter region of this gene lead to a diminished response to antileukotriene drugs used in the treatment of asthma and may also be associated with atherosclerosis and several cancers. Alternatively spliced transcript variants have been observed, but their full-length nature has not been determined.
Image Unavailable-77440-436

Anti-5-Lipoxygenase (Ser524) Rabbit Polyclonal Antibody

Catalog Number: (77440-436)
Supplier: Bioss
Description: This gene encodes a member of the lipoxygenase gene family and plays a dual role in the synthesis of leukotrienes from arachidonic acid. The encoded protein, which is expressed specifically in bone marrow-derived cells, catalyzes the conversion of arachidonic acid to 5(S)-hydroperoxy-6-trans-8,11,14-cis-eicosatetraenoic acid, and further to the allylic epoxide 5(S)-trans-7,9-trans-11,14-cis-eicosatetrenoic acid (leukotriene A4). Leukotrienes are important mediators of a number of inflammatory and allergic conditions. Mutations in the promoter region of this gene lead to a diminished response to antileukotriene drugs used in the treatment of asthma and may also be associated with atherosclerosis and several cancers. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]
Image Unavailable-CAAAA10482-03

3-Hydroxy-4-methoxycinnamic acid predominantly trans ≥98%

Supplier: Thermo Scientific Chemicals
Description: 3-Hydroxy-4-methoxycinnamic acid predominantly trans ≥98%

Certificates

Product Image-89161-692

PKSI-527 ≥95% (by HPLC)

Supplier: Enzo Life Sciences
Description: Highly selective plasma kallikrein inhibitor (Ki = 0.81 µM). Can be used for affinity purification of kalikrein. Suppresses collagen-induced arthritis in a mouse model. Synergizes with NO donors producing antithrombotic effects ex vivo.

Product Image-10109-454

Anti-HAL Rabbit Polyclonal Antibody

Catalog Number: (10109-454)
Supplier: Prosci
Description: HAL is a cytosolic enzyme catalyzing the first reaction in histidine catabolism, the nonoxidative deamination of L-histidine to trans-urocanic acid. HAL defects cause histidinemia which is characterized by increased histidine and histamine and decreased urocanic acid in body fluidsHistidine ammonia-lyase is a cytosolic enzyme catalyzing the first reaction in histidine catabolism, the nonoxidative deamination of L-histidine to trans-urocanic acid. Histidine ammonia-lyase defects cause histidinemia which is characterized by increased histidine and histamine and decreased urocanic acid in body fluids.
Image Unavailable-76082-166

Anti-5-Lipoxygenase Ser271 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (76082-166)
Supplier: Bioss
Description: This gene encodes a member of the lipoxygenase gene family and plays a dual role in the synthesis of leukotrienes from arachidonic acid. The encoded protein, which is expressed specifically in bone marrow-derived cells, catalyzes the conversion of arachidonic acid to 5(S)-hydroperoxy-6-trans-8,11,14-cis-eicosatetraenoic acid, and further to the allylic epoxide 5(S)-trans-7,9-trans-11,14-cis-eicosatetrenoic acid (leukotriene A4). Leukotrienes are important mediators of a number of inflammatory and allergic conditions. Mutations in the promoter region of this gene lead to a diminished response to antileukotriene drugs used in the treatment of asthma and may also be associated with atherosclerosis and several cancers. Alternatively spliced transcript variants have been observed, but their full-length nature has not been determined.
Image Unavailable-C-2015.0025BA

Z-Hyp-OH

Catalog Number: (C-2015.0025BA)
Supplier: Bachem Americas
Description: Sequence: Z-Hyp-OH
Image Unavailable-CA8.20351.0025

Crotonoyl chloride cis- and trans-mixture for synthesis, Sigma-Aldrich®

Catalog Number: (CA8.20351.0025)
Supplier: MilliporeSigma

SDS Certificates


Image Unavailable-TCB0684-500G

meso-Butane-1,2,3,4-tetracarboxylic acid ≥98.0% (by GC, titration analysis)

Supplier: TCI America
Description: CAS Number: 4534-68-3
MDL Number: MFCD00070496
Molecular Formula: C8H10O8
Molecular Weight: 234.16
Purity/Analysis Method: >98.0% (GC,T)
Form: Crystal

SDS

Image Unavailable-CAAAH60144-22

4-Methoxycinnamic acid 99%

Supplier: Thermo Scientific Chemicals

Certificates

Product Image-10103-074

Anti-HAL Rabbit Polyclonal Antibody

Catalog Number: (10103-074)
Supplier: Prosci
Description: HAL is a cytosolic enzyme catalyzing the first reaction in histidine catabolism, the nonoxidative deamination of L-histidine to trans-urocanic acid. HAL defects cause histidinemia which is characterized by increased histidine and histamine and decreased urocanic acid in body fluids Histidine ammonia-lyase is a cytosolic enzyme catalyzing the first reaction in histidine catabolism, the nonoxidative deamination of L-histidine to trans-urocanic acid. Histidine ammonia-lyase defects cause histidinemia which is characterized by increased histidine and histamine and decreased urocanic acid in body fluids.
Product Image-10099-800

Anti-SLC9A7 Rabbit Polyclonal Antibody

Catalog Number: (10099-800)
Supplier: Prosci
Description: Organelles of the secretory and endocytic pathways are distinguished by their luminal acidity, which is generated by the activity of an electrogenic vacuolar-type hydrogen ATPase. Progressive acidification of vesicles in the endocytic pathway is essential for the redistribution and degradation of internalized membrane proteins, such as ligand receptor complexes and fluid-phase solutes. It may play an important role in maintaining cation homeostasis and function of the trans-Golgi network.Organelles of the secretory and endocytic pathways are distinguished by their luminal acidity, which is generated by the activity of an electrogenic vacuolar-type hydrogen ATPase. Progressive acidification of vesicles in the endocytic pathway is essential for the redistribution and degradation of internalized membrane proteins, such as ligand receptor complexes and fluid-phase solutes. This gene is expressed predominantly in the trans-Golgi network, and mediates the influx of sodium or potassium in exchange for hydrogen. It may thus play an important role in maintaining cation homeostasis and function of the trans-Golgi network. This gene is part of a gene cluster on chromosome Xp11.23.Organelles of the secretory and endocytic pathways are distinguished by their luminal acidity, which is generated by the activity of an electrogenic vacuolar-type hydrogen ATPase. Progressive acidification of vesicles in the endocytic pathway is essential for the redistribution and degradation of internalized membrane proteins, such as ligand receptor complexes and fluid-phase solutes. This gene is expressed predominantly in the trans-Golgi network, and mediates the influx of sodium or potassium in exchange for hydrogen. It may thus play an important role in maintaining cation homeostasis and function of the trans-Golgi network. This gene is part of a gene cluster on chromosome Xp11.23.
Image Unavailable-TCT0246-100G

Tiglic acid ≥98.0% (by GC, titration analysis)

Catalog Number: (TCT0246-100G)
Supplier: TCI America
Description: CAS Number: 80-59-1
MDL Number: MFCD00066864
Molecular Formula: C5H8O2
Molecular Weight: 100.12
Purity/Analysis Method: >98.0% (GC,T)
Form: Crystal
Color: White
Boiling point (°C): 82
Melting point (°C): 64
Flash Point (°C): 101
Storage Temperature: 0-10°C

SDS Certificates


Image Unavailable-TCC0359-025G

Ethyl cinnamate ≥99.0%

Supplier: TCI America
Description: CAS Number: 103-36-6
MDL Number: MFCD00009189
Molecular Formula: C11H12O2
Molecular Weight: 176.22
Purity/Analysis Method: >99.0% (GC)
Form: Clear Liquid
Boiling point (°C): 271
Melting point (°C): 10
Flash Point (°C): 137
Specific Gravity (20/20): 1.05

SDS Certificates

Image Unavailable-75789-106

Human Recombinant Cyclophilin C (from E. coli)

Catalog Number: (75789-106)
Supplier: Prosci
Description: Cyclophilin C is an enzyme (EC 5.2.1.8) found in both prokaryotes and eukaryotes that interconverts the cis and trans isomers of peptide bonds with the amino acid proline. Proline has an unusually conformationally restrained peptide bond due to its cyclic structure with its side chain bonded to its secondary amine nitrogen. Most amino acids have a strong energetic preference for the trans peptide bond conformation due to steric hindrance, but prolines unusual structure stabilizes the cis form so that both isomers are populated under biologically relevant conditions. Proteins with prolyl isomerase activity include cyclophilin, FKBPs, and parvulin, although larger proteins can also contain prolyl isomerase domains.
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