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Procurou por: Frascos+lavadores+de+gases


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Descrição: Synthetic peptide, corresponding to amino acids 1130-1180 of Human SHIP1.
Código de Artigo: BWRLBS1321
UOM: 1 * 100 µG
Fornecedor: Bioworld Technology


Descrição: Synthetic peptide, corresponding to amino acids 1180-1230 of Human PLC gamma2.
Código de Artigo: BWRLBS1585
UOM: 1 * 100 µG
Fornecedor: Bioworld Technology


Descrição: Supelpak™-2SV is purified Amberlite® XAD2 that has been specially cleaned and tested for optimal performance in the capturing and extraction of semivolatile organics. Packaged in glass containers.
Código de Artigo: 13674-U
UOM: 1 * 1 unid.
Fornecedor: Merck


Descrição: Welded cleaning tank made of stainless steel. Floating contamination like particles, oil and grease can be removed from the bath surface using an oil separator.
Código de Artigo: 142-1425
UOM: 1 * 1 unid.
Fornecedor: BANDELIN-ELECTRONIC


Descrição: Anatomical poster suitable for wall mounting of the three types of common muscle tissue. 840×1180 mm.
Código de Artigo: 763-0165
UOM: 1 * 1 unid.
Fornecedor: 3B Scientific


Descrição: [EN]AMBERLITE(R) IRA-900 1 * 500 g
Código de Artigo: APOSOR1012271-500G
UOM: 1 * 500 g
Fornecedor: Apollo Scientific

Novo produto


Descrição: DENSI ISO 649 L20 1.160-1.180 : 0.0002 G 1 * 1 unid.
Código de Artigo: ALLA3200LC11620MCA
UOM: 1 * 1 unid.
Fornecedor: Alla France


Descrição: AMBERLITE IRN-150L MIXED BED RESIN 1 * 500 g
Código de Artigo: 551797N
UOM: 1 * 500 g
Fornecedor: VWR Collection


Descrição: DENSI ISO 649 L20 1.180-1.200 : 0.0002 G 1 * 1 unid.
Código de Artigo: ALLA3200LC11820MCA
UOM: 1 * 1 unid.
Fornecedor: Alla France


Descrição: [EN]AMBERLITE(R) IRA-900 1 * 2,5 kg
Código de Artigo: APOSOR1012271-2.5
UOM: 1 * 2,5 kg
Fornecedor: Apollo Scientific

Novo produto


Descrição: [EN]AMBERLITE IRA-67 FREE BASE 1 * 500 g
Código de Artigo: APOSOR1012269-500G
UOM: 1 * 500 g
Fornecedor: Apollo Scientific

Novo produto


Descrição: AMBERLITE IRA-402(CL) ION EXCHANGE RESIN 1 * 25 L
Código de Artigo: B25556.PI
UOM: 1 * 25 L
Fornecedor: Thermo Fisher Scientific

MSDS


Descrição: 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.
Código de Artigo: BOSSBS-11708R-CY5
UOM: 1 * 100 µl
Fornecedor: Bioss


Descrição: 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.
Código de Artigo: BOSSBS-11708R-A555
UOM: 1 * 100 µl
Fornecedor: Bioss


Descrição: 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.
Código de Artigo: BOSSBS-11708R-CY3
UOM: 1 * 100 µl
Fornecedor: Bioss


Descrição: 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.
Código de Artigo: BOSSBS-11708R-FITC
UOM: 1 * 100 µl
Fornecedor: Bioss