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2,2\\\',4,5-Tetrachlorbiphenyl+(PCB+Nr.+48)
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2,2\\\',4,5-Tetrachlorbiphenyl+(PCB+Nr.+48)
Artikel-Nr:
(BURK0310-0010)
Lieferant:
BURKLE
Hersteller-Artikelnummer::
0310-0010
Lokale Artikelnummer::
BURK0310-0010
Beschreibung:
LDPE, translucent.
VE:
1 * 1 ST
Lieferant:
KLINIPATH
Beschreibung:
These ready to use staining solutions are used in histology and cytology staining.
Lieferant:
Sigma-Aldrich
Beschreibung:
Devardas Legierung, Sigma-Aldrich®
Artikel-Nr:
(DELTCP-45H)
Lieferant:
DELTALAB
Hersteller-Artikelnummer::
CP-45H
Lokale Artikelnummer::
DELTCP-45H
Beschreibung:
Staining baskets and racks, made of stainless steel. Designed for 76×26 mm slides.
VE:
1 * 1 ST
Lieferant:
FLUOROCHEM
Beschreibung:
5-Iodisatin
Lieferant:
Sigma-Aldrich
Beschreibung:
Ninhydrin, Sigma-Aldrich®
Artikel-Nr:
(SIALP2278-1G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
P2278-1G
Lokale Artikelnummer::
SIALP2278-1G
Beschreibung:
8-Phenyltheophyllin, Sigma-Aldrich®
VE:
1 * 1 g
Artikel-Nr:
(BOCH8820)
Lieferant:
BOCHEM
Hersteller-Artikelnummer::
8820
Lokale Artikelnummer::
BOCH8820
Beschreibung:
These scoops are made from aluminium.
VE:
1 * 1 ST
Lieferant:
FLUOROCHEM
Beschreibung:
1-Brom-2,3-difluor-5-nitrobenzol
Artikel-Nr:
(BOSSBS-6987R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6987R-HRP
Lokale Artikelnummer::
BOSSBS-6987R-HRP
Beschreibung:
C12orf23 (chromosome 12 open reading frame 23), also known as FLJ11721, FLJ13959 or MGC17943, is a 116 amino acid multi-pass membrane protein belonging to the UPF0444 family. C12orf23 is encoded by a gene located on human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a number of skeletal deformities, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6987R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6987R-A488
Lokale Artikelnummer::
BOSSBS-6987R-A488
Beschreibung:
C12orf23 (chromosome 12 open reading frame 23), also known as FLJ11721, FLJ13959 or MGC17943, is a 116 amino acid multi-pass membrane protein belonging to the UPF0444 family. C12orf23 is encoded by a gene located on human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a number of skeletal deformities, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13247R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13247R-A555
Lokale Artikelnummer::
BOSSBS-13247R-A555
Beschreibung:
Heterotrimeric G proteins function to relay information from cell surface receptors to intracellular effectors. Each of a very broad range of receptors specifically detects an extracellular stimulus (a photon, pheromone, odorant, hormone or neurotransmitter) while the effectors (i.e., adenyl cyclase), which act to generate one or more intracellular messengers, are less numerous. In mammals, G protein Alpha, Beta and Gamma polypeptides are encoded by at least 16, 4 and 7 genes, respectively. Most interest in G proteins has been focused on their Alpha subunits, since these proteins bind and hydrolyze GTP and most obviously regulate the activity of the best studied effectors. Four distinct classes of G Alpha subunits have been identified; these include G Alpha s, G Alpha i, G Alpha q and G Alpha 12/13. The two members of the fourth class of G Alpha subunit proteins, G Alpha 12 and G Alpha 13, are insensitive to ADP-ribosylation by pertussis toxin, share 67% identity with each other and less than 45% identity with other G Alpha subunits and are widely expressed in a broad range of tissues.
VE:
1 * 100 µl
Artikel-Nr:
(FLUO019295-5G)
Lieferant:
FLUOROCHEM
Hersteller-Artikelnummer::
019295-5G
Lokale Artikelnummer::
FLUO019295-5G
Beschreibung:
4',5'-Dimethyl-2'-methoxyacetophenon
VE:
1 * 5 g
 This is a MarketSource item. Additional charges may apply
Lieferant:
HERAEUS
Beschreibung:
Adapter, Centri-Lab, 2x100 ml, Typ C, Tisch-Zentrifuge
Lieferant:
BAILLY
Beschreibung:
Einfache Tupfer für eine Vielzahl von Anwendungen.
Lieferant:
Biotium
Beschreibung:
Recognizes a protein of ~55 kDa, identified as SOX10. This MAb is highly specific and does not cross-react with other members of the SOX-family. SOX genes comprise a family of genes that are related to the mammalian sex-determining gene SRY. These genes similarly contain sequences that encode for the HMG-box domain, which is responsible for the sequence-specific DNA-binding activity. SOX-10 is a sensitive marker of melanoma, including conventional, spindled, and desmoplastic subtypes. It is expressed by metastatic melanomas and nodal capsular nevus in sentinel lymph nodes, but not by other lymph node components such as dendritic cells, which usually express S100 protein. Commonly used melanoma markers, such as anti-HMB-45 and anti-Melan-A, are poorly expressed in desmoplastic melanomas while SOX-10 is moderately to strongly expressed in desmoplastic melanomas. SOX-10 is considered as a very reliable marker for recognizing residual desmoplastic melanomas. In normal tissues, it is expressed in Schwann cells, melanocytes, and myoepithelial cells of salivary, bronchial and mammary glands. SOX-10 expression is also observed in mast cells.
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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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