Sie suchten nach: Amberlite\u00AE+XAD-1180

Lieferant: Thermo Fisher Scientific

Beschreibung: Amberlite® XAD4 Ionenaustauscher

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Lieferant: Thermo Fisher Scientific

Beschreibung: AMBERLITE® IRN-78, Ionenaustauscher (OH-)-Form Ionenaustauscherharz

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Lieferant: Thermo Fisher Scientific

Beschreibung: Amberlite® IRA-410 (Cl) Ionenaustauscherharz

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Lieferant: Thermo Fisher Scientific

Beschreibung: CAS No.: 197809-12-4

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Artikel-Nr: (ACRO465472500)

Lieferant: Thermo Fisher Scientific

Beschreibung: Limonin

UOM: 1 * 250 mg

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Lieferant: Thermo Fisher Scientific

Beschreibung: CAS No.: 9042-11-9

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Lieferant: Thermo Fisher Scientific

Beschreibung: Amberlite® IRA-402 (Cl) Ionenaustauscher

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Lieferant: Thermo Fisher Scientific

Beschreibung: Amberlite® FPC3500 Ionenaustauscherharz

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Lieferant: Thermo Fisher Scientific

Beschreibung: CAS No.: 9050-97-9

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Lieferant: Thermo Fisher Scientific

Beschreibung: CAS No.: 52439-77-7

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Lieferant: Thermo Fisher Scientific

Beschreibung: CAS No.: 9003-69-4

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Lieferant: CleanAir by Baker

Beschreibung: BioVanguard Greenline B is a class II cabinet range which offers simplicity, robustness and high reliability ensuring the highest level of protection for operator, product and the environment, minimising hazards inherent to working with agents assigned to biosafety levels 1, 2 and 3. BioVanguard B is designed for high risk microbiological and high toxic applications, such as the production of cytotoxic medicines.

Artikel-Nr: (BOSSBS-11708R-A647)

Lieferant: Bioss

Beschreibung: ATP13A2 is a 1,180 amino acid multi-pass membrane protein that belongs to the P5 subfamily of ATPases which play an important role in the transportation of inorganic cations. Expressed as multiple alternative spliced isoforms, ATP13A2 functions to catalyze the conversion of ATP to ADP and a free phosphate, thereby participating in the active transport of ions across cellular membranes. Defects in the gene encoding ATP13A2 are the cause of Kufor-Rakeb syndrome (KRS), a rare hereditary type of Parkinson’s disease that exhibits juvenile onset and is characterized by neurodegeneration and dementia. The ATP13A2 gene maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome.

UOM: 1 * 100 µl

Aktion

Artikel-Nr: (BOSSBS-11708R-CY3)

Lieferant: Bioss

Beschreibung: ATP13A2 is a 1,180 amino acid multi-pass membrane protein that belongs to the P5 subfamily of ATPases which play an important role in the transportation of inorganic cations. Expressed as multiple alternative spliced isoforms, ATP13A2 functions to catalyze the conversion of ATP to ADP and a free phosphate, thereby participating in the active transport of ions across cellular membranes. Defects in the gene encoding ATP13A2 are the cause of Kufor-Rakeb syndrome (KRS), a rare hereditary type of Parkinson’s disease that exhibits juvenile onset and is characterized by neurodegeneration and dementia. The ATP13A2 gene maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome.

UOM: 1 * 100 µl

Aktion

Lieferant: Thermo Fisher Scientific

Beschreibung: AMBERLITE® IRN-78, Ionenaustauscher (OH-)-Form nukleare Qualität

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Lieferant: Thermo Fisher Scientific

Beschreibung: Amberlite® IR-120 (Na) Ionenaustauscher

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