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4-Hydroxycyclohexanecarboxylic+acid+(cis+and+trans+mixture)
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4-Hydroxycyclohexanecarboxylic+acid+(cis+and+trans+mixture)
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Xylene (mixture of isomers) with ethylbenzene 99%, AcroSeal® for biochemistry, for histology
Catalog Number:
(76009-510)
Supplier:
Prosci
Description:
NCALD encodes a member of the neuronal calcium sensor (NCS) family of calcium-binding proteins. The protein contains an N-terminal myristoylation signal and four EF-hand calcium binding loops. The protein is cytosolic at resting calcium levels; however, elevated intracellular calcium levels induce a conformational change that exposes the myristoyl group, resulting in protein association with membranes and partial co-localization with the perinuclear trans-golgi network. The protein is thought to be a regulator of G protein-coupled receptor signal transduction. Several alternatively spliced variants of this gene have been determined, all of which encode the same protein; additional variants may exist but their biological validity has not been determined.
Catalog Number:
(75933-840)
Supplier:
Rockland Immunochemical
Description:
LYRM3, also known as NADH dehydrogenase (ubiquinone) 1 beta subcomplex 9 (NDUFB9), is a ubiquitously expressed LYR-motif containing protein. It has been suggested to be a candidate gene for the branchio-oto-renal (BOR) syndrome, which is characterized by branchial and renal abnormalities and heredity deafness disorders. Other than its LYR-motif, LYRM3 appears to have no functional or structural relationship to either LYRM1 or LYRM2.
Supplier:
Adipogen
Description:
Potent anticancer compound. Anti-angiogenic. VEGF, VE-cadherin phosphorylation, matrix metalloproteinase and urokinase-plasminogen activator (uPA) inhibitor. Anti-inflammatory. NF-kappaB inhibitor. Modulates chronic inflammatory diseases, such as type 2 diabetes, rheumatoid arthritis, inflammatory bowel disease. COX-2 and inducible nitric oxide synthase (iNOS; NOS II) inhibitor. Potent antioxidant. Protects cells from lipid peroxidation and DNA damage induced by reactive free radicals. Regulates cancer cell growth, proliferation, transformation, survival, angiogenesis, apoptosis, invasion and metastasis. Chemopreventive. Apoptosis inducer. Promotes cell cycle arrest. Modulates signal transduction pathways including JAK/STAT, MAPK, PI3K/AKT, Wnt and Notch. EGFR and HER-2 receptor signaling inhibitor. MAPKs and activator protein-1 inhibitor. mTOR suppressor. IGF-I signaling inhibitor. Proteasome inhibitor. Telomerase and DNA methyltransferase inhibitor. Selective and noncompetitive HAT inhibitor. Topoisomerase I and II inhibitor. Hedgehog signaling (Hh) modulator. PTCH and Gli1 inhibitor. Wnt signaling inhibitor. Neuroprotective. Activates HO-1 by the ARE/Nrf2 pathway, protecting neurons against oxidative damage. STAT-1 inhibitor. Shows preventive cardiovascular and metabolic (obesity, insulin resistance, hypertension and hypercholesterolemia) effects. Inhibits extracellular signal-related kinases (ERK), activates AMP-activated protein kinase (AMPK), modulates adipocyte marker proteins and down-regulates lipogenic enzymes as well as other potential targets. Fatty acid synthase (FAS) inhibitor. Autophagy stimulator.
Catalog Number:
(10750-688)
Supplier:
Prosci
Description:
GOLPH3 Antibody: GOLPH3 was initially identified as a peripheral membrane protein localized to the trans-Golgi network, but others reported it to be primarily a mitochondrial protein that regulated the mitochondrial mass through the regulation of the mitochondria-specific phospholipid cardiolipin. GOLPH3 has since been implicated in the target of rapamycin (TOR) signalling pathway. Its overexpression in transfected cells led to and increase in anchorage-independent growth and cell proliferation in vitro. Furthermore, GOLPH3-transfected cells enhanced S6 Kinase activity in response to growth factor stimulation by EGF. Simultaneously, AKT phosphorylation increased in these cells, while these events were abrogated in GOLPH3 siRNA treated cells compared to control cells, indicating the GOLPH3 can enhance signalling through TOR-associated complexes. These results suggest that GOLPH3 is a bona fide oncogene and may be a useful target for therapeutic strategies.
Catalog Number:
(EM8.22098.9045)
Supplier:
MilliporeSigma
Description:
MEthylstyrene (mixture of 3- and 4-isomers) stabilised with 4-tert-butylpyrocatechol, CAS no : 1319-73-9, Chemical Formula : 3/4-(CH3)C6H4CH=CH2, Synonyms Vinyltoluene, for synthesis, 45g
Catalog Number:
(TCB4576-50MG)
Supplier:
TCI America
Description:
Bis-PCBM (mixture of isomers), Cas no. 1048679-01-1, Molecular formula: C84H28O4, Form: Crystal- Powder, Colour: Deep yellow - Black, Synonyms: Bis[60]PCBM (mixture of isomers), Size: 50MG
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Hexanes, for analysis, mixture of isomers, Size: 2.5l
Catalog Number:
(EM-HX0080A-20)
Supplier:
MilliporeSigma
Description:
Heptane (mixture of isomers) ≥99% (n-heptane), Supelco®
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Xylene (mixture of isomers) 99% ACS
Catalog Number:
(TS12541-1000)
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Menthone (mixture of isomers) 98%
Supplier:
AMBEED, INC
Description:
Geranyllinalool (mixture of isomers) 97%
Supplier:
AMBEED, INC
Description:
5-Norbornene-2-methylamine (mixture of isomers) 97%
Supplier:
Enzo Life Sciences
Description:
Anti-tumor agent
Catalog Number:
(TCP2393-1G)
Supplier:
TCI America
Description:
Dodecahydrofluorene (mixture of isomers), Purity: >97.0%(GC), CAS Number: 5744-03-6, Molecular Formula: C13H22, Molecular Weight: 178.32, Synonyms: Perhydrofluorene (mixture of isomers), Size: 1G
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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