1,5-Diaminonaphthalin
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-(Boc-aminomethyl)azetidine hydrochloride 96%
Artikel-Nr:
(APOSPC9582-100MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC9582-100MG
Lokale Artikelnummer::
APOSPC9582-100MG
Beschreibung:
1-[3-(Trifluoromethyl)pyridin-2-yl]-1,4-diazepane
VE:
1 * 100 mg
Lieferant:
Thermo Fisher Scientific
Beschreibung:
Establish a leak-tight fit with metric fittings. Nalgene lab-grade, autoclavable clear tubing sets the standard for purity and quality, made from highest-grade resins, free from ortho-phthalate plasticisers.
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Lieferant:
TECAN TRADING
Beschreibung:
Strong cationic exchange chemistry ideal for aggressive cleanup of basic target compounds.
Lieferant:
VWR Collection
Beschreibung:
ND18 Headspace-Fläschchen mit Schraubgewinde und flachem und rundem Boden aus Borosilikatglas der 1. hydrolytischen Klasse. Sie sind mit einer Vielzahl von magnetischen Schraubkappen aus Aluminium und Septenmaterialien erhältlich.
Artikel-Nr:
(BLDPBD00735683-250)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD00735683-250
Lokale Artikelnummer::
BLDPBD00735683-250
Beschreibung:
tert-Butyl 4-(4-amino-2-fluorophenyl)piperidine-1-carboxylate 97%
VE:
1 * 250 mg
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Asymmetric synthesis catalyst; Chiral intermediate for pharmaceuticals and agrochemicals.
Artikel-Nr:
(BOSSBS-10395R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10395R
Lokale Artikelnummer::
BOSSBS-10395R
Beschreibung:
Complexes with metalloproteinases (such as collagenases) and irreversibly inactivates them by binding to their catalytic zinc cofactor. Known to act on MMP-1, MMP-2, MMP-3, MMP-7, MMP-8, MMP-9, MMP-1, MMP-13, MMP-14, MMP-15, MMP-16 and MMP-19.
VE:
1 * 100 µl
Artikel-Nr:
(CONTLWPN0020)
Lieferant:
CONTEC
Hersteller-Artikelnummer::
LWPN0020
Lokale Artikelnummer::
CONTLWPN0020
Beschreibung:
Ideal for wiping exterior surfaces of products and cleaning interior surfaces of process tools or other equipment. Made from 100% textured polyester no-run knit.
VE:
1 * 120 ST
Artikel-Nr:
(BOSSBS-8076R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8076R-CY3
Lokale Artikelnummer::
BOSSBS-8076R-CY3
Beschreibung:
ARRDC1, ARRDC2 (which exists as multiple alternatively spliced isoforms), ARRDC4 and ARRDC5 are arrestin domain-containing proteins that are encoded by genes which map to human chromosomes 9, 15 and 19. Chromosome 9, on which the ARRDC1 gene is localized, contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. The ARRDC2 and ARRDC5 genes map to chromosome 19, which consists of over 63 million bases, houses approximately 1,400 genes and is recognized for having the greatest gene density of the human chromosomes. Unlike other ARRDC genes, the ARRDC4 gene maps to human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD634158-250MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD634158-250MG
Lokale Artikelnummer::
BLDPBD634158-250MG
Beschreibung:
(S)-2-(2-(diphenylphosphino)phenyl)-4-phenyl-4,5-dihydrooxazole 98% 99%ee
VE:
1 * 250 mg
Artikel-Nr:
(BOSSBS-8242R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8242R-A647
Lokale Artikelnummer::
BOSSBS-8242R-A647
Beschreibung:
CTDSPL2 (CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2), also known as HSPC058 or HSPC129, is a 466 amino acid protein that contains one FCP1 homology domain and belongs to the CTDSPL2 family. Existing as two alternatively spliced isoforms, CTDSPL2 is thought to function as a phosphatase and is encoded by a gene that maps to human chromosome 15q15.3. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and comprises about 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
VE:
1 * 100 µl
Lieferant:
USBECK Laborgeräte
Beschreibung:
Tiegel-Deckel, Für Ø: 45 mm, Stärke: 1,5 mm, Eisen
Artikel-Nr:
(BOSSBS-8237R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8237R-CY5
Lokale Artikelnummer::
BOSSBS-8237R-CY5
Beschreibung:
FERM domains are roughly 150 amino acids in length and are found in a number of cytoskeletal-associated proteins such as Ezrin, Radixin, Moesin and 4.1 (erythrocyte membrane protein band 4.1), where they provide a link between cytoskeletal signals and membrane dynamics. FRMD5 (FERM domain-containing protein 5) is a 570 amino acid single-pass membrane protein that contains one FERM domain and exists as two alternatively spliced isoforms. The gene encoding FRMD5 maps to human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8237R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8237R-A750
Lokale Artikelnummer::
BOSSBS-8237R-A750
Beschreibung:
FERM domains are roughly 150 amino acids in length and are found in a number of cytoskeletal-associated proteins such as Ezrin, Radixin, Moesin and 4.1 (erythrocyte membrane protein band 4.1), where they provide a link between cytoskeletal signals and membrane dynamics. FRMD5 (FERM domain-containing protein 5) is a 570 amino acid single-pass membrane protein that contains one FERM domain and exists as two alternatively spliced isoforms. The gene encoding FRMD5 maps to human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localised genes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13222R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13222R-HRP
Lokale Artikelnummer::
BOSSBS-13222R-HRP
Beschreibung:
FSD2 is a 749 amino acid protein containing one B30.2/SPRY domain and two fibronectin type-III domains. The gene encoding FSD2 maps to human chromosome 15q25.2. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and consists of about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are also associated with chromosome 15.
VE:
1 * 100 µl
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