(Tetrahydropyran-4-yl)methyl+tosylate
Catalog Number:
(10712-352)
Supplier:
Abnova
Description:
Mouse monoclonal antibody raised against partial recombinant ERBB3.
Supplier:
MP Biomedicals
Description:
Zincon is a colorimetric indicator for Zn, Cu and Hg. Reagent for the spectrophotometric determination of zinc. Simultaneous determination of zinc and copper. Used in automated flow injection analysis of zinc. As a metal indicator for EDTA titration of Zn, or for the back titration of Ca in the presence of Mg with glycoletherdiaminetertraacetic acid (GEDTA or EGTA).
Catalog Number:
(10267-978)
Supplier:
Bioss
Description:
Nrarp (NOTCH-regulated ankyrin repeat protein) is a 114 amino acid protein that contains two ANK repeats and is thought to play a role in the formation of somites. The gene encoding Nrarp maps to human chromosome 9, which contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia and Familial dysautonomia are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in translocations that lead to the aberrant production of a BCR-ABL fusion protein often found in leukemias.
Catalog Number:
(10298-066)
Supplier:
Bioss
Description:
Glutathione (GSH) is a tripeptide antioxidant which reduces disulfide bonds between cytoplasmic proteins. The constitutive enzyme glutathione reductase transforms glutathione into its reduced state which ultimately can provide a measure of cellular toxicity. GSTT2 (glutathione S-transferase theta-2), also known as GST class-theta-2, is a 244 amino acid enzyme with sulfatase activity that functions in conjugating reduced glutathione to hydrophobic electrophiles. GSTT2 exists as a homodimer in the cytoplasm and is expressed in low levels in the liver and the lung. GSTT2 belongs to the GST superfamily and contains both a GST C-terminal and a GST N-terminal domain. The gene encoding GSTT2 exists on human chromosome 22.
Supplier:
Thermo Scientific Chemicals
Description:
(1S,2S)-(-)-1,2-Diamino-1,2-diphenylethane (1S,2S)-(-)-1,2-Diphenylethylenediamine. Grade: 97. Melting Point C79-81*. Boiling Point C: NA. C14H16N2. 29841-69-8. IRRITANT KEEP COLD AIR SENSITIVE
Catalog Number:
(76109-510)
Supplier:
Bioss
Description:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases, such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD22 (ankyrin repeat domain 22) is a 191 amino acid protein that contains four ANK repeats. Conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, ANKRD22 is encoded by a gene that maps to human chromosome 10. Chromosome 10 encodes nearly 1,200 genes within 135 million bases, making up approximately 4.5% of the human genome. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman?s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Catalog Number:
(76107-346)
Supplier:
Bioss
Description:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases, such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD22 (ankyrin repeat domain 22) is a 191 amino acid protein that contains four ANK repeats. Conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, ANKRD22 is encoded by a gene that maps to human chromosome 10. Chromosome 10 encodes nearly 1,200 genes within 135 million bases, making up approximately 4.5% of the human genome. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman?s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Supplier:
BeanTown Chemical
Description:
CAS: 5437-45-6; EC No: 226-611-4; MDL No: MFCD00000190; RTECS: AF5957215
Liquid; Linear Formula: C6H5CH2CO2CH2Br ; Molecular Formula: C9H9BrO2; MW: 229.07
Boiling Point: 166-170°/22 mmHg; Flash point: <gt/>110°C (<gt/>230°F)
Density (g/mL): 1.446; Refractive Index: 1.544
Catalog Number:
(10668-462)
Supplier:
Bioss
Description:
Tripartite motif-containing protein 3 (TRIM3), also known as RING finger protein 22 (RNF22), RING finger protein 97 (RNF97) or brain-expressed RING finger protein (BERP), is a 744 amino acid member of the TRIM family, also known as the RING-B-box coiled-coil (RBCC) family. Members of the RBCC family have an N-terminal RING finger, followed by one or two zinc-binding domains (B-box domains), a leucine coiled-coil region and a variable C-terminal domain. Localized to cytoplasmic filaments, TRIM3 has been shown to interact with å-actinin-4 and myosin V, two proteins associated with the actin cytoskeleton. Specifically, å-actinin-4 interacts with the RBCC domain of TRIM3, and the C-terminal tail of Myosin V interacts with with the unique C-terminal ∫-propeller domain of TRIM3. These associations suggest that TRIM3 may play a role in cell motility and cargo transport. Three named isoforms of TRIM3 exist as a result of alternative splicing events.
Catalog Number:
(10434-060)
Supplier:
Bioss
Description:
EMP-2 is a 167 amino acid multi-pass membrane protein that contains four-transmembrane domains and belongs to the GAS3/PMP22 (growth arrest-specific-3/peripheral myelin protein-22) family. Localized to lipid raft domains in the plasma membrane, EMP-2 regulates the expression of several target proteins and is necessary for blastocyst implantation in the uterine endometrium. Specifically, EMP-2 mediates blastocyst implantation by controlling the cell membrane expression of MHC and glycosylphosphatidylinositol-anchored proteins, as well as Integrins and caveolin-1. In adult tissues, EMP-2 is expressed in heart, lung, ovary and intestine, while fetal expression is highest in kidney, brain and liver. Overexpression of EMP-2 is associated with endometrial adenocarcinoma, suggesting a possible role for EMP-2 in tumorigenesis.
Supplier:
AMBEED, INC
Description:
(1R,2S)-2-Fluorocyclopropanamine-4-methylbenzenesulfonate 97%
Supplier:
Thermo Scientific Chemicals
Description:
Transition interval: pH 4.6 (yellow) to pH 6.0 (red)
Supplier:
AMBEED, INC
Description:
(2S,4S)-2,4-Dimethylazetidine hydrochloride ≥97%
Catalog Number:
(PI37615)
Supplier:
Invitrogen
Description:
ABTS substrate is a water-soluble peroxidase substrate that yields a measurable green end product for use in ELISA methods.
Supplier:
APOLLO SCIENTIFIC
Description:
(2S)-(-)-3,3,3-Trifluoro-1,2-propenoxide 97%
Supplier:
Matrix Scientific
Description:
Methyl (2S,4S)-4-[3-(acetylamino)phenoxy]-2-pyrrolidinecarboxylate hydrochloride
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