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2-(2,2,2-Trifluoroethoxy)ethanamine+hydrochloride
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2-(2,2,2-Trifluoroethoxy)ethanamine+hydrochloride
Artikel-Nr:
(USBIC2398-69G)
Lieferant:
US Biological
Hersteller-Artikelnummer::
C2398-69G
Lokale Artikelnummer::
USBIC2398-69G
Beschreibung:
Anti-CD44 Rat Monoclonal Antibody (PE (Phycoerythrin)) [clone: 5K255]
VE:
1 * 100 µG
Artikel-Nr:
(HONE12257.9050)
Lieferant:
Honeywell Chemicals
Hersteller-Artikelnummer::
12257.9050
Lokale Artikelnummer::
HONE12257.9050
Beschreibung:
Kaliumdichromat
VE:
1 * 50 kg
Lieferant:
FOAMTEC
Beschreibung:
UltraMOP™ III mop heads are constructed of a snag-resistant, polyester fabric laminated to an absorbent polyurethane foam employing the patent pending Bump-PROOF® design. The Bump-PROOF® design improves cleanliness and durability as the durable fabric extends over the front and rear edges making it ideal for ISO class 4 and 5 clean rooms.
Artikel-Nr:
(PRSI48-415)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
48-415
Lokale Artikelnummer::
PRSI48-415
Beschreibung:
Human group III secreted phospholipase A2 belongs to a superfamily of intracellular and secreted enzymes that catalyze the hydrolysis of glycerophospholipids at the sn-2 position to release fatty acids and lysophospholipids. Group III PLA2 enzymes were originally identified in invertebrates such as bees and scorpions. Human group III sPLA2 has been shown to be a calcium dependent enzyme. It consists of a central group III sPLA2 domain flanked by unique N- and C-terminal domains that are proteolytically removed in most tissues. The sPLA2 domain is sufficient for catalytic activity. SPLA2-III is preferentially expressed in the microvascular endothelium of tissues with inflammation, ischemic injury and cancer.
VE:
1 * 50 µG
Lieferant:
Merck
Beschreibung:
Kaliumiodid 99,0-100,5% (durch argentometrische Titration, an Trockenmasse), EMPROVE® api Ph. Eur., BP, JP, USP, SAFC®
Artikel-Nr:
(BOSSBS-3008R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3008R-FITC
Lokale Artikelnummer::
BOSSBS-3008R-FITC
Beschreibung:
The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the `pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders. Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions. ADCA is caused by the expansion of the CAG repeats, producing an elongated polyglutamine tract in the corresponding protein. The expanded repeats are variable in size and unstable, usually increasing in size when transmitted to successive generations. The function of the ataxins is not known. This locus has been mapped to chromosome 6, and it has been determined that the diseased allele contains41-81 CAG repeats, compared to 6-39 in the normal allele, and is associated with spinocerebellar ataxia type 1 (SCA1). At least two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq].
VE:
1 * 100 µl
Lieferant:
MACRON AVANTOR BRAND
Beschreibung:
EDTA Dinatriumsalz Dihydrat 99,0-101,0% (Trockenmasse), GenAR® USP für die Biotechnologie, Macron Fine Chemicals™
Artikel-Nr:
(HONE01717.9025)
Lieferant:
Honeywell Chemicals
Hersteller-Artikelnummer::
01717.9025
Lokale Artikelnummer::
HONE01717.9025
Beschreibung:
Kaliumhexafluorotitanat
VE:
1 * 25 kg
Lieferant:
Bel-Art Products, a Part of SP
Beschreibung:
These lightweight pipetting devices made of PP are designed for quick and accurate one-handed operation. Available in three colour-coded pipette volumes.
Lieferant:
Spectrum Chemical
Beschreibung:
Form: Granular
Artikel-Nr:
(BELAF379040025)
Lieferant:
Bel-Art Products, a Part of SP
Hersteller-Artikelnummer::
F379040025
Lokale Artikelnummer::
BELAF379040025
Beschreibung:
These lightweight pipetting devices made of PP can be used with glass and plastic pipettes up to 2, 10 or 25 ml. Designed for quick and accurate one-handed operation.
VE:
1 * 1 ST
Lieferant:
BIOLEGEND INC
Beschreibung:
Anti-Synapsin I/II/III Mouse Monoclonal Antibody [clone: A17080A] (Alexa Fluor® 647)
Artikel-Nr:
(SIAL208965-25G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
208965-25G
Lokale Artikelnummer::
SIAL208965-25G
Beschreibung:
Trinatriumhexafluoroferrat, Sigma-Aldrich®
VE:
1 * 25 g
Artikel-Nr:
(BSBTPA1439)
Lieferant:
BosterBio
Hersteller-Artikelnummer::
PA1439
Lokale Artikelnummer::
BSBTPA1439
Beschreibung:
Rabbit IgG polyclonal antibody for Carbonic anhydrase 3(CA3) detection. Tested with WB, IHC-P in Human; Mouse; Rat.
VE:
1 * 0,1 mg
Artikel-Nr:
(SIAL366595-1G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
366595-1G
Lokale Artikelnummer::
SIAL366595-1G
Beschreibung:
di-Kaliumhexachlororhenat, Sigma-Aldrich®
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-3008R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3008R-A750
Lokale Artikelnummer::
BOSSBS-3008R-A750
Beschreibung:
The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterised by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the `pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders. Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions. ADCA is caused by the expansion of the CAG repeats, producing an elongated polyglutamine tract in the corresponding protein. The expanded repeats are variable in size and unstable, usually increasing in size when transmitted to successive generations. The function of the ataxins is not known. This locus has been mapped to chromosome 6, and it has been determined that the diseased allele contains41-81 CAG repeats, compared to 6-39 in the normal allele, and is associated with spinocerebellar ataxia type 1 (SCA1). At least two transcript variants encoding the same protein have been found for this gene.
VE:
1 * 100 µl
Preis auf Anfrage
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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