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1,4-Cyclohexanedicarboxylic+acid+(mixture+of+cis+and+trans+isomer
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1,4-Cyclohexanedicarboxylic+acid+(mixture+of+cis+and+trans+isomer
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Catalog Number:
(10670-156)
Supplier:
Bioss
Description:
The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in protein-protein interactions and protein-DNA interactions. Specifically, they are thought to be involved in the ubiquitination pathway of protein degradation. RNF165 (RING finger protein 165) is a 346 amino acid protein that contains one RING-type zinc finger. Via its RING-type zinc finger, RNF165 may play a role in transcriptional regulation and protein degradation events. The gene encoding RNF165 maps to human chromosome 18, which houses over 300 genes, including Trisomy 18, or Edwards syndrome, the second most common trisomy after Downs syndrome. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are also associated with chromosome 18.
Catalog Number:
(77677-379)
Supplier:
LGC STANDARDS
Description:
Carbamate Pesticides Mixture 638 100 µg/mL in Methanol, Dr. Ehrenstorfer, LGC Standards
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
cis-3-Hexen-1-ol 98%
Supplier:
TCI America
Description:
CAS Number: 28679-16-5
MDL Number: MFCD00040422
Molecular Formula: C11H18N2O2
Molecular Weight: 210.28
Purity/Analysis Method: <gt/>97.0% (GC)
Form: Clear Liquid
Color: Colorless
Specific Gravity (20/20): 1.02
Storage Temperature: 0-10°C
Catalog Number:
(102891-546)
Catalog Number:
(10073-062)
Supplier:
Prosci
Description:
GDF-5 is expressed in long bones during embryonic development and postnatally in articular cartilage. Mutations in the GDF-5 gene have been implicated in Grebe Syndrome, which is characterized by short stature, extra digits, short and deformed extremities, and in Hunter-Thompson type dwarfism. The mature and functional form of GDF-5 is a homodimer of two 120 amino-acid polypeptide chain (monomers) linked by a single disulfide bond. Each GDF-5 monomer is expressed as the C-terminal part of a precursor polypeptide, which also contains a 27 amino-acid signal peptide and a 348 amino-acid propeptide. This precursor undergoes intracellular dimerization, and upon secretion it is processed by a furin-type protease. Recombinant murine GDF-5 is a 27.0 kDa homodimeric disulfide-linked protein consisting of two 120 amino acids.
Supplier:
Thermo Scientific Chemicals
Description:
cis-4-(Benzyloxycarbonylamino)cyclohexanecarboxaldehyde, 97%
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
cis-2-Aminomethyl-1-cyclohexanol hydrochloride 99%
Supplier:
MP Biomedicals
Description:
Spermidine is a biogenic polyamine formed from putrescine. It is essential in both normal and neoplastic tissue growth. It plays an important role in the regulation of cellular proliferation and differentiation. Forms stable compounds with nucleic acids. Inhibits neuronal nitric oxide synthase (nNOS).
Catalog Number:
(10277-096)
Supplier:
Bioss
Description:
Glycosyltransferases that mediate the regio- and stereoselective transfer of sugars, such as the fucosyltransferases, determine cell surface-carbohydrate profiles, which are essential interfaces for biological recognition processes. Fucosyltransferases (FucTs) catalyze the covalent association of fucose to different positional linkages on sugar acceptor molecules. The carbohydrate moieties that are generated are covalently attached to cell surfaces and are necessary to ensure a surface contour that satisfies a variety of physiological roles. FucT-XI is a 492 amino acid single-pass type II membrane protein that belongs to the glycosyltransferase 10 family. Localizing to Golgi apparatus, FucT-XI may act as a fucosyltransferase and exists as two alternatively spliced isoforms. The gene encoding FucT-XI maps to mouse chromosome 14 A3.
Catalog Number:
(10277-064)
Supplier:
Bioss
Description:
Glycosyltransferases that mediate the regio- and stereoselective transfer of sugars, such as the fucosyltransferases, determine cell surface-carbohydrate profiles, which are essential interfaces for biological recognition processes. Fucosyltransferases (FucTs) catalyze the covalent association of fucose to different positional linkages on sugar acceptor molecules. The carbohydrate moieties that are generated are covalently attached to cell surfaces and are necessary to ensure a surface contour that satisfies a variety of physiological roles. FucT-XI is a 492 amino acid single-pass type II membrane protein that belongs to the glycosyltransferase 10 family. Localizing to Golgi apparatus, FucT-XI may act as a fucosyltransferase and exists as two alternatively spliced isoforms. The gene encoding FucT-XI maps to mouse chromosome 14 A3.
Catalog Number:
(10748-684)
Supplier:
Prosci
Description:
LIS1 Antibody: Lissencephaly is a severe brain developmental disease characterized by the mislocalization of cortical neurons, a smooth cerebral surface, mental retardation, and seizures. Classical lissencephaly is caused by sporadic mutations in the LIS1 gene. While LIS1 is known to act in a pathway deactivating the lipid messenger platelet-activating factor, LIS1 forms a complex with Nudel and 14-3-3epsilon which is then transported from neuronal cell bodies through the actions of DISC1 and KIF5A, a microtubule-dependent directed motor protein kinesin. Decreased expression of LIS1 blocked neural stem cell division, morphogenesis, and motility, suggesting that LIS1 plays an important role in neuronal cell proliferation and localization in the developing brain. At least two isoforms of LIS1 are known to exist.
Supplier:
TCI America
Description:
cis-Octahydroisoindole, Purity: >97.0%(GC)(T), CAS Number: 1470-99-1, Molecular Formula: C8H15N, Molecular Weight: 125.22, Size: 1G
Catalog Number:
(10295-752)
Supplier:
Bioss
Description:
GBE1 is a 702 amino acid protein that is expressed at high levels in muscle and liver and is involved in glycogen biosynthesis. Existing as a monomer, GBE1 catalyzes the transfer of alpha-1,4-linked glucosyl units from the outer end of a glycogen chain to an alpha-1,6 position on a neighboring glycogen chain and, via this catalytic activity, plays an essential role in glycogen accumulation. Defects in the gene encoding GBE1 are the cause of glycogen storage disease type 4 (GSD4) and adult polyglucosan body disease (APBD), the first of which is a metabolic disorder that is associated with the accumulation of polysaccharides and is characterized by liver disease during childhood. Unlike GSD4, APBD is a late-onset disorder that affects the central and peripheral nervous systems and is characterized by cognitive impairment, pyramidal tetraparesis and peripheral neuropathy.
Catalog Number:
(77693-768)
Supplier:
LGC STANDARDS
Description:
N-Acetyl-S-(3,4-dihydroxybutyl)-L-cysteine-d7 (Mixture of Diastereomers), TRC, LGC Standards
Supplier:
AMBEED, INC
Description:
cis-6-Nonen-1-ol 98%
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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.
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