You Searched For: Magnesium+citrate+hydrate

Catalog Number: (BOSSBS-12039R-HRP)

Supplier: Bioss

Description: GDE1 is a 331 amino acid multi-pass membrane protein that localizes to both the membrane and the cytoplasm and contains one GDPD domain. Expressed in a wide variety of tissues, GDE1 uses magnesium as a cofactor to catalyze the conversion of 1-(sn-glycero-3-phospho)-1D-myo-inositol to myo-inositol and sn-glycerol 3-phosphate, an event that is modulated by G protein signaling pathways and provides a link between phosphoinositide metabolism and G protein signal transduction. The gene encoding GDE1 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-9433R-A350)

Supplier: Bioss

Description: FIGNL1 is a 674 amino acid protein belonging to the AAA ATPase family. FIGNL1 exists as a hexamer that undergoes alternative splicing to produce two isoforms. FIGNL1 utilizes magnesium as a cofactor and is phosphorylated upon DNA damage, probably by ATM or ATR. FIGNL1 is suggested to regulate osteoblast proliferation and differentiation. FIGNL1 is encoded by a gene located on human chromosome 7, which consists about 158 milllion bases, encodes over 1000 genes and makes up about 5% of the human genome. 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.

UOM: 1 * 100 µl

Catalog Number: (D9015-100MG)

Supplier: SIGMA ALDRICH MICROSCOPY

Description: 3,3′-Diaminobenzidine tetrahydrochloride hydrate has been used in immunohistological staining procedure and <i>in situ</i> hybridisation. DAB (3,3′-Diaminobenzidine) is utilised in many applications for the visualisation of peroxidase activity. In the peroxidase reaction, DAB serves as a hydrogen donor in the presence of peroxide. The oxidised DAB forms an insoluble brown end-product for use in immunohistological and immunoblotting staining procedures.

UOM: 1 * 100 mg

Catalog Number: (BIRBORB99236-96)

Supplier: Biorbyt

Description: Mouse E-Selectin ELISA Kit for the quantitative detection of mouse soluble E-Selectin in cell culture supernates, serum and plasma (heparin, citrate).

UOM: 1 * 96 items

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Supplier: Lovibond Tintometer

Description: Test kit, VARIO manganese citrate buffer F10 (powder pack), Range: 0 - 20 mg/L Mn, For unit: MD 600

Supplier: SIGMA ALDRICH MICROSCOPY

Description: Morin hydrate is a yellowish pigment and a fluorescent indicator. It is used for the fluorimetric determination of several metals, mostly aluminum. Morin has been utilised in fluorescent microscopy as a fluorescent nuclear stain and as an application to detect aluminium in the brain by demonstrating metal salts.

Catalog Number: (BOSSBS-9734R-A647)

Supplier: Bioss

Description: The phosphorylation and dephosphorylation of proteins on serine and threonine residues is an essential means of regulating a broad range of cellular functions in eukaryotes, including cell division, homeostasis and apoptosis. A group of proteins that are intimately involved in this process are the serine/threonine (Ser/Thr) protein kinases. TSSK 6 (testis-specific serine kinase 6), also known as SSTK, TSSK4, FKSG82 or CT72, is a 273 amino acid protein that contains one protein kinase domain and belongs to the Ser/Thr protein kinase family. Highly expressed in testis with lower expression in ovary, colon, thymus, small intestine and spleen, TSSK 6 catalyzes the ATP-dependent phosphorylation of proteins involved in sperm production and chromatin remodeling. TSSK 6 uses magnesium as a cofactor and is thought to be required for proper sperm development and function, as well as DNA condensation events. Defects in the gene encoding TSSK 6 are associated with male infertility characterized by low sperm count and decreased sperm motility.

UOM: 1 * 100 µl

Catalog Number: (20636.183)

Supplier: VWR Chemicals

Description: Phosphotungstic acid hydrate, AnalaR NORMAPUR® analytical reagent sodium-free

UOM: 1 * 100 g

MSDS Certificates

Supplier: Alfa Aesar

Description: γ-Cyclodextrine hydrate

Catalog Number: (APOSPC5633-1G)

Supplier: APOLLO SCIENTIFIC

Description: 4-Fluorophenylglyoxal hydrate

UOM: 1 * 1 g

Supplier: VWR Chemicals

Description: Dodecamolybdophosphoric acid hydrate, AnalaR NORMAPUR® ACS, Reag. Ph. Eur. analytical reagent

MSDS

Catalog Number: (24248.292)

Supplier: VWR Chemicals

Description: Iron(III) sulphate hydrate, GPR RECTAPUR®

UOM: 1 * 1 kg

MSDS Certificates

Catalog Number: (PRSI26-819)

Supplier: ProSci Inc.

Description: HSPA4L possesses chaperone activity in vitro where it inhibits aggregation of citrate synthase.

UOM: 1 * 50 µG

Supplier: Alfa Aesar

Description: β-Cyclodextrine hydrate

Catalog Number: (Q0501-10MG)

Supplier: SIGMA ALDRICH MICROSCOPY

Description: Calcium-specific chelator and indicator. Upon binding calcium there is a shift in the UV spectrum and an enhancement of fluorescence.

UOM: 1 * 10 mg

Catalog Number: (PERCN2025330)

Supplier: PERKIN ELMER GC INSTRUMENTS

Description: Hollow cathode lamp, Atomax™, For: Non Perkin-Elmer instruments, Magnesium

UOM: 1 * 1 items