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Ethyl+3-(2-aminophenyl)acrylate
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Ethyl+3-(2-aminophenyl)acrylate
Artikel-Nr:
(HECH42990014)
Lieferant:
GLASWARENFABRIK KARL HECHT
Hersteller-Artikelnummer::
42990014
Lokale Artikelnummer::
HECH42990014
Beschreibung:
High-density polyethylene.
VE:
1 * 1 ST
Lieferant:
Sigma-Aldrich
Beschreibung:
2,5-Dibromtoluol, Sigma-Aldrich®
Artikel-Nr:
(PRSI76-204)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
76-204
Lokale Artikelnummer::
PRSI76-204
Beschreibung:
The MEL-14 monoclonal antibody specifically reacts with L- selectin (CD62L), a receptor with lectin-like and Epidermal Growth Factor-like domains. The weight of the CD62L molecules depend on their origin: 74 kDa (on lymphocytes) or 95 kDa (on neutrophils).In the Mouseorganism, CD62L can be expressed by most thymocytes, on subsets of B and T lymphocytes, monocytes, eosinophils, and neutrophils. The L-selectin binds sulfated, fucosylated, and glycosylated glycoproteins (MadCAM-1, GLYCAM-1, and CD 34). It mediates the migration of lymphocytes to the site of inflammation and their return to the peripheral lymphoid tissues and to the HEV (high endothelial venules). In vitro, L-selectin inhibits this binding and the lymphocyte extravasation into peripheral lymph nodes.
VE:
1 * 0,025 mg
New Product
Lieferant:
Sigma-Aldrich
Beschreibung:
Tricyclohexylphosphin, Sigma-Aldrich®
Lieferant:
GLASWARENFABRIK KARL HECHT
Beschreibung:
Borosilicate glass highly resistant cover glasses with precise and faultless cut.
Artikel-Nr:
(SCOT242620609)
Lieferant:
DWK Life Sciences
Hersteller-Artikelnummer::
242620609
Lokale Artikelnummer::
SCOT242620609
Beschreibung:
DURAN® borosilicate glass 3.3. clear. Angled at 75° with ground joint cone.
VE:
1 * 1 ST
Artikel-Nr:
(201-1601)
Lieferant:
WITEG LABORTECHNIK
Hersteller-Artikelnummer::
0.182.014
Lokale Artikelnummer::
WITG0.182.014
Beschreibung:
Borosilicate glass 3.3.
VE:
1 * 1 ST
Artikel-Nr:
(J60592.06)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
J60592.06
Lokale Artikelnummer::
ALFAJ60592.06
Beschreibung:
1,3-Dihydroxyaceton dimer
VE:
1 * 5 g
Artikel-Nr:
(VARI6610001800)
Lieferant:
VARIAN
Hersteller-Artikelnummer::
6610001800
Lokale Artikelnummer::
VARI6610001800
Beschreibung:
Fluorescence cuvettes designed for UV/visible analysis in routine applications of molecular spectroscopy.
VE:
1 * 1 ST
Artikel-Nr:
(LENZ01101714)
Lieferant:
Lenz Laborglas GmbH & CO.KG
Hersteller-Artikelnummer::
01101714
Lokale Artikelnummer::
LENZ01101714
Beschreibung:
Sleeves, made of PTFE. For fitting onto standard ground cones.
VE:
1 * 1 ST
Lieferant:
Sigma-Aldrich
Beschreibung:
4-Pyridon, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-9680R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9680R-A680
Lokale Artikelnummer::
BOSSBS-9680R-A680
Beschreibung:
C19orf28, also known as PP3501, is a multi-pass membrane protein that belongs to the major facilitator superfamily. The gene encoding C19orf28 localizes to chromosome 19 and, due to alternative splicing events, C19orf28 exists as two isoforms. Consisting of around 63 million bases with over 1400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognised for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The C19orf28 gene product has been provisionally designated C19orf28 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9680R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9680R-A488
Lokale Artikelnummer::
BOSSBS-9680R-A488
Beschreibung:
C19orf28, also known as PP3501, is a multi-pass membrane protein that belongs to the major facilitator superfamily. The gene encoding C19orf28 localizes to chromosome 19 and, due to alternative splicing events, C19orf28 exists as two isoforms. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The C19orf28 gene product has been provisionally designated C19orf28 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9680R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9680R-A350
Lokale Artikelnummer::
BOSSBS-9680R-A350
Beschreibung:
C19orf28, also known as PP3501, is a multi-pass membrane protein that belongs to the major facilitator superfamily. The gene encoding C19orf28 localizes to chromosome 19 and, due to alternative splicing events, C19orf28 exists as two isoforms. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The C19orf28 gene product has been provisionally designated C19orf28 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-3626R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3626R-CY3
Lokale Artikelnummer::
BOSSBS-3626R-CY3
Beschreibung:
Protein kinase C (PKC) is a family of serine- and threonine-specific protein kinases that can be activated by calcium and second messenger diacylglycerol. PKC family members phosphorylate a wide variety of protein targets and are known to be involved in diverse cellular signaling pathways. PKC also serve as major receptors for phorbol esters, a class of tumor promoters. Each member of the PKC family has a specific expression profile and is believed to play distinct roles in cells. The protein encoded by this gene is one of the PKC family members. There have been at least 12 different PKC isoforms identified in humans to date including alpha, beta I, beta II, gamma, delta, epsilon, zeta, eta, theta, iota, lambda, and mu. PKC gamma is expressed solely in the brain and spinal cord and its localization is restricted to neurons. It has been demonstrated that several neuronal functions, including long term potentiation (LTP) and long term depression (LTD), specifically require this kinase. Knockout studies in mice also suggest that this kinase may be involved in neuropathic pain development. Defects in this protein have been associated with neurodegenerative disorder spinocerebellar ataxia-14 (SCA14).
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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