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Magnesium Phosphate, Reference Standard (AS)

Référence Produit: (1374292.)
Fournisseur: USP
Description: USP Reference Standards are specified for use in conducting official USP–NF tests and assays. USP also provides Reference Standards specified in the Food Chemicals Codex as well as authentic substances—high-quality chemical samples—as a service to analytical, clinical, pharmaceutical and research laboratories. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.
UOM: 1 * 2 g
Product Image-HYCLSH30013.03

Dulbecco's phosphate buffered saline (DPBS), for cell culture, powder format, HyClone™

Fournisseur: HyClone products (Cytiva)
Description: Balanced salt solution used for multiple cell culture applications (powder form).

Product Image-ACRO423720030

Ammonium-fer (II) sulfate hexahydraté 99% ACS

Fournisseur: Thermo Fisher Scientific
Description: Ammonium-fer (II) sulfate hexahydraté 99% ACS

FDS (Fiche de données de sécurité) Certificats.

Image Unavailable-4876-5

Nitro-4 phényle phosphate sel de sodium hexahydraté (pNPP), Sigma-Aldrich®

Fournisseur: Merck Millipore (Oncogene)
Description: Nitro-4 phényle phosphate sel de sodium hexahydraté (pNPP), Sigma-Aldrich®

Image Unavailable-MOLE35359763-25G

Nitro-4 phényle phosphate sel de sodium hexahydraté (pNPP)

Référence Produit: (MOLE35359763-25G)
Fournisseur: Molekula
Description: Nitro-4 phényle phosphate sel de sodium hexahydraté (pNPP)
UOM: 1 * 25 g

Market Source Item This is a MarketSource item. Additional charges may apply

Image Unavailable-J61401.KN

Nitro-4 phényle phosphate sel de sodium hexahydraté (pNPP) 5 mg, en comprimés

Référence Produit: (J61401.KN)
Fournisseur: Thermo Fisher Scientific
Description: Substrate for alkaline and acid phosphatase determinations.
UOM: 1 * 100 Pce

FDS (Fiche de données de sécurité) Certificats.


Image Unavailable-ICNA0210087810

Nitro-4 phényle phosphate sel de sodium hexahydraté (pNPP), en poudre

Fournisseur: MP Biomedicals
Description: p nitrophenol is the substrate of choice for use with alkaline phosphatase in ELISA procedures. This substrate produces a soluble end product that is yellow in color and can be read spectrophotometrically at 405 nm. The pNPP reaction may be stopped with 3 M NaOH and read at 405 nm.

FDS (Fiche de données de sécurité)

Image Unavailable-1029986.

Ammonium Phosphate Dibasic, Reference Standard

Référence Produit: (1029986.)
Fournisseur: USP
Description: USP Reference Standards are specified for use in conducting official USP–NF tests and assays. USP also provides Reference Standards specified in the Food Chemicals Codex as well as authentic substances—high-quality chemical samples—as a service to analytical, clinical, pharmaceutical and research laboratories. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.
UOM: 1 * 1 g
Image Unavailable-PIER34047

Nitro-4 phényle phosphate sel de sodium hexahydraté (pNPP) 5 mg, en comprimés

Référence Produit: (PIER34047)
Fournisseur: Thermo Fisher Scientific
Description: Nitro-4 phényle phosphate sel de sodium hexahydraté (pNPP) 5 mg, en comprimés
UOM: 1 * 105 Tablet
Image Unavailable-ICNA114027812

Dehydrated culture media, YNB media, MP Biomedicals

Fournisseur: MP Biomedicals
Description: YNB media, a component of synthetic defined yeast media is a well defined composition of salts, vitamins and nitrogen source for a vigorous growth of <i>S. cerevisiae</i>.

Image Unavailable-BOSSBS-12039R-CY5

Anti-GDE1 Rabbit Polyclonal Antibody (Cy5®)

Référence Produit: (BOSSBS-12039R-CY5)
Fournisseur: 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
Image Unavailable-BOSSBS-12039R-A488

Anti-GDE1 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Référence Produit: (BOSSBS-12039R-A488)
Fournisseur: 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
Image Unavailable-BOSSBS-12039R

Anti-GDE1 Rabbit Polyclonal Antibody

Référence Produit: (BOSSBS-12039R)
Fournisseur: 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
Image Unavailable-BOSSBS-12039R-FITC

Anti-GDE1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Référence Produit: (BOSSBS-12039R-FITC)
Fournisseur: 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
Image Unavailable-BOSSBS-12039R-A350

Anti-GDE1 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Référence Produit: (BOSSBS-12039R-A350)
Fournisseur: 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
Image Unavailable-BOSSBS-12039R-A750

Anti-MIR16/GDE1 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Référence Produit: (BOSSBS-12039R-A750)
Fournisseur: 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 catalyse 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 Signalling 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 characterised 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
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