Indium(III)+phosphate
Catalog Number:
(10299-392)
Supplier:
Bioss
Description:
Esterifies acyl-group from acyl-ACP to the sn-1 position of glycerol-3-phosphate, an essential step in glycerolipid biosynthesis.
Catalog Number:
(ABCA_AB224820-100U)
Supplier:
ABCAM INC.
Description:
Anti-DNA Ligase III/LIG3 Rabbit Polyclonal Antibody
Catalog Number:
(10392-056)
Supplier:
Bioss
Description:
Transaldolase 1 is a key enzyme of the nonoxidative pentose phosphate pathway providing ribose-5-phosphate for nucleic acid synthesis and NADPH for lipid biosynthesis. This pathway can also maintain glutathione at a reduced state and thus protect sulfhydryl groups and cellular integrity from oxygen radicals. The functional gene of transaldolase 1 is located on chromosome 11 and a pseudogene is identified on chromosome 1 but there are conflicting map locations. The second and third exon of this gene were developed by insertion of a retrotransposable element. This gene is thought to be involved in multiple sclerosis.
Catalog Number:
(10481-746)
Supplier:
Bioss
Description:
Dephosphorylates pseudouridine 5'-phosphate, a potential intermediate in rRNA degradation. Pseudouridine is then excreted intact in urine.
Supplier:
General Laboratory Products
Description:
For use as a diluent in microbial limit testing of food and water.
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Catalog Number:
(10465-898)
Supplier:
Bioss
Description:
Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate. Inhibitor of p53-induced apoptosis.Tissue specificity: Expressed at a moderately low level in many tissues. Most abundant in kidney, prostate, ovary, intestine, and spleen.
Catalog Number:
(10299-390)
Supplier:
Bioss
Description:
Esterifies acyl-group from acyl-ACP to the sn-1 position of glycerol-3-phosphate, an essential step in glycerolipid biosynthesis.
Supplier:
BeanTown Chemical
Description:
CAS: 13775-53-6; EC No: 237-410-6; MDL No: MFCD00003507; RTECS: BD0075000
UN No: UN3260; Haz Class: 8; Packing Group: III
Powder; Linear Formula: Na3AlF6; MW: 209.95
Melting Point: 1000°
Density (g/mL): 2.90
Catalog Number:
(ABCA_AB231084-100U)
Supplier:
ABCAM INC.
Description:
Anti-beta III Tubulin Mouse Monoclonal Antibody [clone: 5G8]
Catalog Number:
(ABCA_AB264113-100U)
Supplier:
ABCAM INC.
Description:
Anti-beta III Tubulin Mouse Monoclonal Antibody [clone: 5G8]
Supplier:
CHEMetrics
Description:
Ideal for low- to medium-range colorimetric analysis of water quality
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Supplier:
MilliporeSigma
Description:
For use with Midas* III Stainer (15204-300).
Catalog Number:
(77520-344)
Supplier:
AFG BIOSCIENCE LLC
Description:
Rat AngIII (Angiotensin III) ELISA Kit
Catalog Number:
(10293-680)
Supplier:
Bioss
Description:
Fibronectins are multi-domain glycoproteins that bind to a variety of substances including collagen, actin, heparin, DNA, fibrin and fibronectin receptors. They are involved in a diverse array of important functions such as blood coagulation, wound healing, cell adhesion, cell differentiation and migration. FNDC4 (Fibronectin type III domain-containing protein 4), also known as FRCP1 (Fibronectin type III repeat-containing protein 1), is a 234 amino acid membrane protein that contains one fibronectin type-III domain, which serves as a binding site for DNA, heparin or the cell surface. The gene encoding FNDC4 is localized to human chromosome two, which houses over 1,400 genes and comprises nearly 8% of the human genome.
Catalog Number:
(10390-240)
Supplier:
Bioss
Description:
Cytochrome C Oxidase subunits I, II and III form the functional core of the enzyme complex.Defects in Cytochrome C Oxidase subunits III are a cause of Leber hereditary optic neuropathy (LHON) and cytochrome c oxidase deficiency (COX deficiency). Defects in Cytochrome C Oxidase subunits III are also found in mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome and recurrent myoglobinuria.
Catalog Number:
(10390-238)
Supplier:
Bioss
Description:
Cytochrome C Oxidase subunits I, II and III form the functional core of the enzyme complex.Defects in Cytochrome C Oxidase subunits III are a cause of Leber hereditary optic neuropathy (LHON) and cytochrome c oxidase deficiency (COX deficiency). Defects in Cytochrome C Oxidase subunits III are also found in mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome and recurrent myoglobinuria.
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