Hledali jste: Amberlite\u00AE+XAD-1180

Dodavatel: Thermo Fisher Scientific

Popis: CAS No.: 9003-69-4

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Dodavatel: Thermo Fisher Scientific

Popis: Amberlite® IRA-410 (Cl) ion-exchange resin

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Dodavatel: Thermo Fisher Scientific

Popis: CAS No.: 197809-12-4

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Dodavatel: Thermo Fisher Scientific

Popis: CAS No.: 9042-11-9

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Dodavatel: Thermo Fisher Scientific

Popis: CAS No.: 9050-97-9

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Dodavatel: Thermo Fisher Scientific

Popis: Amberlite® IR-120 (Na) ion exchange resin

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Dodavatel: Thermo Fisher Scientific

Popis: Amberlite® IRA-200C (Na) ion exchange resin

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Dodavatel: Thermo Fisher Scientific

Popis: Amberlite® IRA-402 (Cl) ion exchange resin

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Dodavatel: Thermo Fisher Scientific

Popis: Amberlite® IRN-78, Ion exchange resin cationic type (OH-) ion-exchange resin

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Dodavatel: Thermo Fisher Scientific

Popis: Amberlite® IRN-77, ion exchange resin cationic type (H⁺) nuclear grade

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Dodavatel: Thermo Fisher Scientific

Popis: CAS No.: 52439-77-7

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Dodavatel: Thermo Fisher Scientific

Popis: Amberlite® IRN-78, Ion exchange resin cationic type (OH-) nuclear grade

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Katalogové číslo: (BWRLBS1585)

Dodavatel: Bioworld Technology

Popis: Synthetic peptide, corresponding to amino acids 1180-1230 of Human PLC gamma2.

Měrná jednotka: 1 * 100 µG

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Katalogové číslo: (ACRO465472500)

Dodavatel: Thermo Fisher Scientific

Popis: Limonin

Měrná jednotka: 1 * 250 mg

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Dodavatel: CleanAir by Baker

Popis: 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.

Katalogové číslo: (BOSSBS-11708R-A555)

Dodavatel: Bioss

Popis: 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.

Měrná jednotka: 1 * 100 µl

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