2-Bromo-3-(methoxymethoxy)pyridine
Catalog Number:
(100503-788)
Supplier:
Electron Microscopy Sciences
Description:
Crystal Violet is used for Gram positive/Gram negative bacteria, filaments, Holzer's method for glial fibers, Amyloid in pathological human tissue, and determining chromatin and nucleoli in plant tissue.
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Catalog Number:
(77034-670)
Supplier:
AMBEED, INC
Description:
1-(((6R,7R)-7-((Z)-2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-(methoxyimino)acetamido)-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl)methyl)imidazo[1,2-b]pyridazin-1-ium chloride 98%
Supplier:
Strem Chemicals Inc
Description:
Metal Beta-diketonates, Volatile Precursors for CVD
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 044447-5G , MDL Number: MFCD00215151
Catalog Number:
(17788-090)
Supplier:
Encompass
Description:
These basic lab coats are available in three different lengths.
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Catalog Number:
(103658-878)
Supplier:
Sino Biological
Description:
This antibody was obtained from a rabbit immunized with purified, recombinant Mouse CD53 (rM CD53; Catalog#50722-M07H; Q61451; Glu107-Asn181).
Supplier:
Dickies
Description:
Dickies® style C7988, regular fit, straight leg. Jean-style work pant which sits slightly below waist.
Catalog Number:
(15566-083)
Supplier:
Chemplex
Description:
A 44µm powder well suited for blending and as a diluent for high concentrations. Well balanced with abrasive and lubricious constituents for grinding most sample materials emphasizing difficult-to-process samples requiring long grinding cycles in metallic comminution vials or dishes. Resistant to degradation by thermal and irradiation exposure. Samples have “plasticized” surfaces. Available in bulk powder and ½ gm pre-weighed tablets for ease of dispensing.
Catalog Number:
(76171-608)
Supplier:
Boster Biological Technology
Description:
Rabbit IgG polyclonal antibody for Neuronal acetylcholine receptor subunit alpha-5(CHRNA5) detection. Tested with WB, IHC-P in Human;Mouse;Rat.
Supplier:
Biotium
Description:
This antibody recognizes a protein of 12 kDa, identified asβ2-microglobulin.β2-microglobulin non-covalently associates with the 44 kDa chain to form the HLA Class I antigen complex. Human β2-microglobulin associated with HLA Class I antigens is expressed on many types of cells including lymphocytes, thymocytes, monocytes, granulocytes, platelets, endothelial cells, and epithelial cells. It is absent on erythrocytes. This MAb is specific to human β2-microglobulin and does not react with non-human primate cells. This antibody reacts with all cell types excluding erythrocytes. The detection of β2-microglobulin in body fluids has been used as a tumor marker and for monitoring patients with HIV infection. Clone 246 E9.E7 is the same as HLA.ABC.m2.
CF® dyes are Biotium's next-generation fluorescent dyes. CF®405S is a blue fluorescent dye (Ex/Em 404/431 nm) with superior brightness compared to other blue dyes; it is also compatible with super-resolution imaging by SIM. Note: Conjugates of blue fluorescent dyes are not recommended for detecting low abundance targets, because blue dyes have lower fluorescence and can give higher non-specific background than other dye colors.
Supplier:
BeanTown Chemical
Description:
CAS: 115-39-9; EC No: 204-086-2; MDL No: MFCD00005875; RTECS: SJ7453000
Crystalline; Molecular Formula: C19H10Br4O5S; MW: 669.96
Melting Point: 273° (decomposes)
Catalog Number:
(103280-486)
Supplier:
Novus Biologicals
Description:
The CEP44 Antibody from Novus Biologicals is a rabbit polyclonal antibody to CEP44. This antibody reacts with human. The CEP44 Antibody has been validated for the following applications: Immunohistochemistry, Immunohistochemistry-Paraffin.
Supplier:
Biotium
Description:
The mouse monoclonal antibody recognizes CD1b, a 44 kDa type I glycoprotein associated with beta2-microglobulin. It is expressed on dendritic cells, Langerhans cells, thymocytes, and T acute lymphoblastic leukemia cells. The CD1 multigene family encodes five forms of the CD1 T-cell surface glycoprotein in human, designated CD1A, 1B, 1C, 1D and 1E. CD1, a type 1 membrane protein, has structural similarity to the MHC class I antigen and has been shown to present lipid antigens for recognition by T lymphocytes. Constitutive endocytosis of CD1B molecules and the differential sorting of MHC class II from lysosomes separate peptide- and lipid antigen-presenting molecules during dendritic cell maturation. CD1B is also expressed in interdigitating cells.
CF® dyes are Biotium's next-generation fluorescent dyes. CF®488A is a green fluorescent dye (Ex/Em 490/515 nm) with excellent brightness and photostability. The dye is minimally charged for less non-specific binding. CF®488A also is compatible with super-resolution imaging by TIRF.
Catalog Number:
(10313-110)
Supplier:
Bioss
Description:
Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf44 gene product has been provisionally designated C7orf44 pending further characterization.
Supplier:
MP Biomedicals
Description:
Carnitine is a quaternary amine that occurs naturally in most mammalian tissue.
It is present in relatively high concentrations in skeletal muscle and heart where it is involved in regulating energy metabolism. It shifts glucose metabolism from glycolysis to glycogen storage and enhances the transport of long chain fatty acids into the mitochondria where they are oxidized for energy production. Store at Room Temperature(15-30 °C), desiccate
Catalog Number:
(10313-108)
Supplier:
Bioss
Description:
Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf44 gene product has been provisionally designated C7orf44 pending further characterization.
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