Wyszukano: Amberlite®+XAD-1180

Numer katalogowy: (BOSSBS-11708R-A647)

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

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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

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Numer katalogowy: (763-0149)

Producent: 3B Scientific

Opis: This poster is mounted on a reel.

j.m.: 1 * 1 SZT

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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

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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

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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

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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

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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.

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

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Producent: Thermo Fisher Scientific

Opis: Amberlite® HPR4200 (Cl) ion-exchange resin

New Product

Numer katalogowy: (763-0150)

Producent: 3B Scientific

Opis: This poster is mounted on a reel.

j.m.: 1 * 1 SZT

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 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

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Numer katalogowy: (GERI0011)

Producent: GERING

Opis: Density hydrometers with reference temperature of 20 °C.

j.m.: 1 * 1 SZT

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Numer katalogowy: (763-0162)

Producent: 3B Scientific

Opis: Plank mounted on roll. 84×118 cm.

j.m.: 1 * 1 SZT

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 This is a MarketSource item. Additional charges may apply

Numer katalogowy: (BOSSBS-11708R)

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

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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

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 This is a MarketSource item. Additional charges may apply