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Indium(III)+phosphate


16,623  results were found

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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
New Product
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.

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.
Minority or Woman-Owned Business Enterprise
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.
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
MSDS SDS

Supplier:  ABCAM INC.
Description:   Anti-beta III Tubulin Mouse Monoclonal Antibody [clone: 5G8]
New Product

Supplier:  ABCAM INC.
Description:   Anti-beta III Tubulin Mouse Monoclonal Antibody [clone: 5G8]
New Product
Supplier:  CHEMetrics
Description:   Ideal for low- to medium-range colorimetric analysis of water quality
MSDS SDS
Small Business Enterprise
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
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.

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.

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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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 call is still displayed and you need assistance, please call us at 1-800-932-5000.
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 call 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
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
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The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at 1-800-932-5000.
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