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Numer katalogowy: (BOSSBS-11708R-CY5)
Producent: Bioss
Opis: 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.
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-11708R-A680)
Producent: Bioss
Opis: ATP13A2 is a 1180 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 catalyse 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 characterised by neurodegeneration and dementia. The ATP13A2 gene maps to human chromosome 1, which spans 260 million base pairs, contains over 3000 genes and comprises nearly 8% of the human genome.
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-11708R-CY3)
Producent: Bioss
Opis: 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.
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-11708R-A488)
Producent: Bioss
Opis: 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.
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-11708R-CY7)
Producent: Bioss
Opis: 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.
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-11708R-FITC)
Producent: Bioss
Opis: 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.
j.m.: 1 * 100 µl


Numer katalogowy: (763-0149)
Producent: 3B Scientific
Opis: This poster is mounted on a reel.
j.m.: 1 * 1 SZT

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

Numer katalogowy: (763-0150)
Producent: 3B Scientific
Opis: This poster is mounted on a reel.
j.m.: 1 * 1 SZT

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

Numer katalogowy: (763-0158)
Producent: 3B Scientific
Opis: This poster is mounted on a reel.
j.m.: 1 * 1 SZT

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

Numer katalogowy: (BOSSBS-11708R-A750)
Producent: Bioss
Opis: ATP13A2 is a 1180 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 catalyse 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 characterised by neurodegeneration and dementia. The ATP13A2 gene maps to human chromosome 1, which spans 260 million base pairs, contains over 3000 genes and comprises nearly 8% of the human genome.
j.m.: 1 * 100 µl


Numer katalogowy: (GERI0011)
Producent: GERING
Opis: Density hydrometers with reference temperature of 20 °C.
j.m.: 1 * 1 SZT

New Product


Numer katalogowy: (763-0162)
Producent: 3B Scientific
Opis: Plank mounted on roll. 84×118 cm.
j.m.: 1 * 1 SZT

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

Producent: CleanAir by Baker
Opis: BioVanguard Green Line is a Class II cabinet range which offers simplicity, robustness and high reliability and ensures the highest level of protection for the operator, product and environment, minimising the hazards inherent with working with agents assigned to biosafety levels one, two and three. It is designed for microbiological research with biological agents (e.g. bacteria, viruses, etc) and allergens.

Producent: Thermo Fisher Scientific
Opis: Amberlite® HPR4200 (Cl) ion-exchange resin

New Product

Numer katalogowy: (BINH1001204)
Producent: 3B Scientific
Opis: This oversized anatomical chart illustrates the process of human birth in anatomical detail.
j.m.: 1 * 1 SZT

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

Numer katalogowy: (763-0165)
Producent: 3B Scientific
Opis: Anatomical poster suitable for wall mounting of the three types of common muscle tissue. 840×1180 mm.
j.m.: 1 * 1 SZT

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

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Zapasy tego artykułu są ograniczone, ale możliwe, że jest on dostępny w pobliskim magazynie. Upewnij się, że jesteś zalogowany na stronie, aby móc sprawdzić dostępność zapasów. Jeśli call ciągle się wyświetla i potrzebujesz pomocy, zadzwoń na 58 323 82 00.
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