U heeft gezocht op: VX-702

Leverancier: TCI

Omschrijving: VX-702 ≥98.0% (by HPLC)

Catalogus nummer: (APOSBISN0171-10MG)

Leverancier: Apollo Scientific

Omschrijving: MAPK/ERK Signalling Pathway

UOM: 1 * 10 mg

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Leverancier: Apollo Scientific

Omschrijving: MAPK/ERK Signalling Pathway

Leverancier: Apollo Scientific

Omschrijving: MAPK/ERK Signalling Pathway

Leverancier: Merck

Omschrijving: Puur- en ultrapuur-watersysteem, Quantum VX-ultrazuiveringpatroon zonder Millipak-eindfilter

Catalogus nummer: (PRSI10-695)

Leverancier: ProSci Inc.

Omschrijving: Anti-VX-15 Recombinant Antibody

UOM: 1 * 0,1 mg

New Product Sale

Catalogus nummer: (APOSBITP1905-1MG)

Leverancier: Apollo Scientific

Omschrijving: Recombinant HIV-2 gp36 (390-702)

UOM: 1 * 1 mg

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Leverancier: Thermo Fisher Scientific

Omschrijving: 2-(4-Methoxyphenyl)ethanol ≥98%

MSDS Certificaten

Leverancier: TCI

Omschrijving: 1,3-Dimethyladamantane ≥99.0% (by GC)

Catalogus nummer: (TCIAP0597-25G)

Leverancier: TCI

Omschrijving: Acid blue 1

UOM: 1 * 25 g

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Catalogus nummer: (BWRLBS5813)

Leverancier: Bioworld Technology

Omschrijving: Synthetic peptide, corresponding to amino acids 702-747 of Human Na+ CP type IXalpha.

UOM: 1 * 1 EA

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Leverancier: Ansell

Omschrijving: Besides providing excellent cut and abrasion protection and a firm grip, especially in dry and slightly oily environments, EDGE® 48-702 microfoam nitrile gloves also ensure higher tactile sensitivity and dexterity compared to foam nitrile gloves.

Catalogus nummer: (213-0483)

Leverancier: VWR Collection

Omschrijving: Gemaakt van PMP (TPX), kristalhelder.

UOM: 1 * 6 ST

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Catalogus nummer: (BOSSBS-13300R-A555)

Leverancier: Bioss

Omschrijving: GBE1 is a 702 amino acid protein that is expressed at high levels in muscle and liver and is involved in glycogen biosynthesis. Existing as a monomer, GBE1 catalyzes the transfer of alpha-1,4-linked glucosyl units from the outer end of a glycogen chain to an alpha-1,6 position on a neighboring glycogen chain and, via this catalytic activity, plays an essential role in glycogen accumulation. Defects in the gene encoding GBE1 are the cause of glycogen storage disease type 4 (GSD4) and adult polyglucosan body disease (APBD), the first of which is a metabolic disorder that is associated with the accumulation of polysaccharides and is characterized by liver disease during childhood. Unlike GSD4, APBD is a late-onset disorder that affects the central and peripheral nervous systems and is characterized by cognitive impairment, pyramidal tetraparesis and peripheral neuropathy.

UOM: 1 * 100 µl

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Catalogus nummer: (BOSSBS-13300R-CY5)

Leverancier: Bioss

Omschrijving: GBE1 is a 702 amino acid protein that is expressed at high levels in muscle and liver and is involved in glycogen biosynthesis. Existing as a monomer, GBE1 catalyzes the transfer of alpha-1,4-linked glucosyl units from the outer end of a glycogen chain to an alpha-1,6 position on a neighboring glycogen chain and, via this catalytic activity, plays an essential role in glycogen accumulation. Defects in the gene encoding GBE1 are the cause of glycogen storage disease type 4 (GSD4) and adult polyglucosan body disease (APBD), the first of which is a metabolic disorder that is associated with the accumulation of polysaccharides and is characterized by liver disease during childhood. Unlike GSD4, APBD is a late-onset disorder that affects the central and peripheral nervous systems and is characterized by cognitive impairment, pyramidal tetraparesis and peripheral neuropathy.

UOM: 1 * 100 µl

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Catalogus nummer: (APOSOR471172-5G)

Leverancier: Apollo Scientific

Omschrijving: 7-Methyl-1,4-dioxaspiro[4.5]decan-8-one

UOM: 1 * 5 g

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