Text Search >
Indium(III)+phosphate
Print…
You Searched For:
17,193 results were found
Indium(III)+phosphate
Catalog Number:
(89354-556)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to POLR3A (polymerase (RNA) III (DNA directed) polypeptide A, 155kDa)
Catalog Number:
(103636-878)
Supplier:
Sino Biological
Description:
A DNA sequence encoding the domain III of the West Nile virus (WNV)((lineage 1, strain NY99) envelope glycoprotein (E)
(ABA62343.1) (Gln586-Ala705) was expressed with a polyhistidine tag at the C-terminus. 
Catalog Number:
(10486-412)
Supplier:
Bioss
Description:
Repair polymerase that plays a key role in base-excision repair. Has 5'-deoxyribose-5-phosphate lyase (dRP lyase) activity that removes the 5' sugar phosphate and also acts as a DNA polymerase that adds one nucleotide to the 3' end of the arising single-nucleotide gap. Conducts 'gap-filling' DNA synthesis in a stepwise distributive fashion rather than in a processive fashion as for other DNA polymerases.
Supplier:
Cayman Chemical Company
Description:
BMS 345541 (trifluoroacetate salt), Purity >/=98%, MF: C14H17N5.2CF3COOH, MW: 483.4, Synonyms: IKK Inhibitor III, N1-(1,8-dimethylimidazo[1,2-a]quinoxalin-4-yl)-1,2-ethanediamine, trifluoroacetate salt, Formulation: crystalline, Storage: -20C, Size: 10mg
Catalog Number:
(10241-848)
Supplier:
Bioss
Description:
Can degrade fibronectin, laminin, gelatins of type I, III, IV, and V; collagens III, IV, X, and IX, and cartilage proteoglycans. Activates procollagenase.
Catalog Number:
(102552-916)
Supplier:
BioVendor
Description:
FGF-23 is a secreted, nonglycosylated monomeric protein belonging to the FGF family. Full-lenght FGF-23 is a phosphaturic hormone which blocks neural phosphate reabsorbtion. Upon processing, biologically inactive N- and C- terminal fragments are generated. Defects in FGF-23 is associated with autosomal dominant hypophosphatemic rickets. The FGF-23 gene encodes a member of the fibroblast growth factor family that is mutant in autosomal dominant hypophosphatemic rickets (ADHR). Tumor-induced osteomalacia is one of the paraneoplastic disorders characterized by hypophosphatemia caused by renal phosphate wasting. The fact that removal of responsible tumors normalizes phosphate metabolism is evidence that a humoral phosphaturic factor, sometimes called phosphatonin, is the basis of tumor-induced osteomalacia. Thus, overproduction of FGF-23 causes tumor-induced osteomalacia, whereas mutations in the FGF-23 gene result in autosomal hypophosphatemic rickets possibly by preventing proteolytic cleavage, which enhances the biologic activity of FGF-23. The mutations in FGF-23 found in ADHR lie within 3 nucleotides of each other in the proprotein convertase cleavage site. Jonsson et al. (2003) showed that FGF-23 is readily detectable in the plasma or serum of healthy persons and can be markedly elevated in those with oncogenic osteomalacia or X-linked hypophosphatemia, suggesting that this growth factor has a role in phosphate homeostasis.
Supplier:
BeanTown Chemical
Description:
CAS: 656-64-4; MDL No: MFCD03788559
UN No: UN2811; Haz Class: 6.1; Packing Group: III
Solid; Molecular Formula: C6H5BrFN; MW: 190.01
Melting Point: 34-37°
Catalog Number:
(89156-726)
Supplier:
Enzo Life Sciences
Description:
Antibiotic possessing weak<i> in vitro</i> antimicrobial activity against gram positive bacteria and fungi
Catalog Number:
(10266-044)
Supplier:
Bioss
Description:
The endophilins comprise a family of three SH3 domain-containing proteins designated Endophilin I, II and III, or alternatively known as SH3P4, SH3P8 and SH3P13, respectively. These proteins associate with Amphiphysin, Synaptojanin and Dynamin and are implicated in presynaptic vesicle trafficking at nerve terminals. The expression patterns of the endophilins are consistent with their cellular functions at the neuronal synapse, as Endophilin I is ex- pressed only in the brain. Both Endophilin II and Endophilin III are detected in a variety of tissues. Endophilin I is also implicated in modulating G protein-coupled receptor signaling by functioning as an adapter protein and directing 1 adrenergic receptors to the endocytic machinery.
Catalog Number:
(EM8.20099.0250)
Supplier:
BeanTown Chemical
Description:
CAS: 18759-96-1; EC No: 414-570-7; MDL No: MFCD00211072
UN No: UN3259; Haz Class: 8; Packing Group: III
Solid; Linear Formula: H2NC6H4CH2NHCH3; Molecular Formula: C8H12N2; MW: 136.19
Catalog Number:
(103617-482)
Supplier:
Sino Biological
Description:
This antibody was obtained from a rabbit immunized with purified, recombinant Human Carbonic Anhydrase III / CA3 (rh Carbonic Anhydrase III / CA3; Catalog#10503-H08E; NP_005172.1; Met1-Lys260).
Catalog Number:
(10785-152)
Supplier:
CHI Scientific
Description:
Kit, Human Ovary OptiTDS* 1, PrimaCell* Tissue Dissociation System, A mixture of collagenase I, collagenase III, collagenase IV, collagenase, and trypsin, Stability: package should be stored at -20 degree Celcius, and effective up to 4 months
Catalog Number:
(10081-294)
Supplier:
Proteintech
Description:
ENTPD8, also named as UNQ2492 and PRO5779, belongs to the GDA1/CD39 NTPase family. ENTPD8 is a canalicular ectonucleoside NTPDase which responsible for the main hepatic NTPDase activity. Ectonucleoside NTPDases catalyze the hydrolyzis of gamma- and beta-phosphate residues of nucleotides, playing a central role in concentration of extracellular nucleotides. Has activity toward ATP, ADP, UTP and UDP, but not toward AMP. ENTPD8 catalyze the reaction :ATP + 2 H2O = AMP + 2 phosphate.
Catalog Number:
(10392-058)
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.
Inquire for Price
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.
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.
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.
This product has been blocked by your organization. Please contact your purchasing department for more information.
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.
|
|||||||||
List View
