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Image Unavailable-BNUM0862-50

Anti-GPC3 Mouse Monoclonal Antibody (Purified, BSA-free) [clone: 1G12]

Katalogové číslo: (BNUM0862-50)
Dodavatel: Biotium
Popis: Recognizes a protein, which is identified as HGAL. It contains a putative PDZ-interacting domain, an immunoreceptor tyrosine-based activation motif (ITAM), and two putative SH2 binding sites. In B cells, its expression is specifically induced by interleukin-4. HGAL is specifically expressed in germinal center B-cells, but is absent in mantle and marginal zone B-cells and in the inter-follicular and para-cortical regions in normal tonsils and lymph nodes. Its high degree of specificity for germinal center B-cells makes anti-HGAL an ideal marker for the detection of germinal center-derived B-cell lymphomas. HGAL expression has been used to help elucidate nodal marginal zone lymphoma (NMZL) from cases of diffuse follicle center lymphoma. Additionally, HGAL expression was shown to correlate with survival in patients with diffuse large B-cell lymphoma (DLBCL).
Měrná jednotka: 1 * 50 µl
Image Unavailable-BNUM0096-50

Anti-H1 Mouse Monoclonal Antibody (Purified, BSA-free) [clone: AE-4]

Katalogové číslo: (BNUM0096-50)
Dodavatel: Biotium
Popis: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.
Měrná jednotka: 1 * 50 µl
Image Unavailable-705-0989

Water sampler, BU2000

Katalogové číslo: (705-0989)
Dodavatel: Hach
Popis: Portable water sampler using pressure-vacuum technology. Combines small dimensions by offering the 24×1 l bottle option for glass as well as plastic bottles or 25 l composite PE bottle. Enables the option of 24×1 l or 1×25 l PE sample bottles, respectively 24×1 l or 1×20 l glass sample bottles, in combination with an active cooled sampler base. This is especially interesting for sampling in accordance to local regulation (24 × hourly mixed sample/daily mixed sample). Cleaning efforts are reduced to a minimum due to the new designed vat sample distributor and the standard round sample bottles. The sampler offers two cooling options for ensuring a sample storage at 4 °C: passive with ice packs or active with an integrated cooling machine including autarkic temperature control. The pressure-vacuum sampler is ISO 5667 compliant. To avoid cross contamination, the system is purged before and after each sample is taken. The compact, weatherproof housing made of PE plastic ensures failure-free operation over many years and often changing installation locations. Even in extremely corrosive applications. All programming features of stationary sampler products are available.
Měrná jednotka: 1 * 1 KS
Image Unavailable-BOSSBS-11708R-CY7

Anti-ATP13A2 Rabbit Polyclonal Antibody (Cy7®)

Katalogové číslo: (BOSSBS-11708R-CY7)
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
Product Image-392-0265

96- and 384-well cell culture microplates, Advanced TC™

Dodavatel: Greiner Bio-One
Popis: Microplates with a modified culture surface to optimise cell characteristics and functions. The improved adherence and increased growth rate improve and accelerate cell proliferation. Additionally, the Advanced TC™ surface facilitates uniform and consistent cell adherence, increases throughput and reduces cell loss, for example during automated washing stages. Free of detectable DNase, RNase and human DNA.

Environmentally Preferable

Image Unavailable-ENZOALX430127M005

KN-93 phosphate ≥98% (by 1H-NMR)

Dodavatel: ENZO LIFE SCIENCES
Popis: CaM kinase II inhibitor

Image Unavailable-BOSSBS-11708R-CY5

Anti-ATP13A2 Rabbit Polyclonal Antibody (Cy5®)

Katalogové číslo: (BOSSBS-11708R-CY5)
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
Image Unavailable-BOSSBS-11708R

Anti-ATP13A2 Rabbit Polyclonal Antibody

Katalogové číslo: (BOSSBS-11708R)
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
Image Unavailable-BOSSBS-11708R-FITC

Anti-ATP13A2 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Katalogové číslo: (BOSSBS-11708R-FITC)
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
Image Unavailable-ENZOALX270440M005

AMI-1 ≥98% (by 1H-NMR, HPLC)

Katalogové číslo: (ENZOALX270440M005)
Dodavatel: ENZO LIFE SCIENCES
Popis: PRMT inhibitor
Měrná jednotka: 1 * 5 mg
Image Unavailable-42570.30

Silikagel, Pore size: 60 Å ≥99.5% (metals basis) 0.040-0.063 mm (230-400 mesh)

Dodavatel: Thermo Fisher Scientific
Popis: Silikagel, Pore size: 60 Å ≥99.5% (metals basis) 0.040-0.063 mm (230-400 mesh)

Bezpečnostní list Certifikáty

Image Unavailable-ICNA02101459.5

Cytidine free base, white powder

Dodavatel: MP Biomedicals
Popis: Soluble in water.

Product Image-PIER37570

Pierce™ Blocking Buffers, Protein Free

Katalogové číslo: (PIER37570)
Dodavatel: Thermo Fisher Scientific
Popis: These protein-free blocking buffers are either a PBS or a TBS formulation of a non protein compound that provides effective blocking for membrane based and plate based protein detection methods, resulting in extremely low background.
Měrná jednotka: 1 * 1 L
Image Unavailable-BOSSBS-11708R-A750

Anti-PARK9/ATP13A2 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Katalogové číslo: (BOSSBS-11708R-A750)
Dodavatel: Bioss
Popis: 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.
Měrná jednotka: 1 * 100 µl
Product Image-ICNA113060012

Casamino Acids, MP Biomedicals

Dodavatel: MP Biomedicals
Popis: Casamino acids is supplemented to microbiological growth media.

Image Unavailable-BOSSBS-11708R-A555

Anti-ATP13A2 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

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
Cena na vyžádání
Omezené množství produktu na skladě. Zboží může být k dispozici v jiném skladě poblíž vašeho sídla. Přesvědčte se, že jste přihlášení na stránky, abyste mohli vidět dostupné položky na skladě. Pokud je stále zobrazeno call a potřebujete asistenci, volejte na číslo 321 570 321.
Omezené množství produktu na skladě. Zboží může být k dispozici v jiném skladě poblíž vašeho sídla. Přesvědčte se, že jste přihlášení na stránky, abyste mohli vidět dostupné položky na skladě. Pokud je stále zobrazeno call a potřebujete asistenci, volejte na číslo 321 570 321.
Daná chemikálie je regulována dle platné legislativy a bude vyžadováno vyplnění formuláře. Jeho včasným vyplněním uspíšíte dodání produktu.
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Tento produkt již není k dispozici. Podobné produkty můžete vyhledat pomocí VWR katalogových čísel nebo čísel dodavatele uvedených výše. Pokud potřebujete další asistenci, zavolejte na telefonní číslo zákaznického servisu VWR 321 570 321.
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