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(3,4-Dimethoxyphenyl)essigsäurehydrazid
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(3,4-Dimethoxyphenyl)essigsäurehydrazid
Artikel-Nr:
(1.00383.9025)
Lieferant:
Merck
Hersteller-Artikelnummer::
1.00383.9025
Lokale Artikelnummer::
MERP1.00383.9025
Beschreibung:
DL-Aplfelsäure, EMPROVE® ESSENTIAL Ph. Eur., NF, FCC, E296, SAFC®
VE:
1 * 25 kg
Artikel-Nr:
(FLUO023161-1G)
Lieferant:
FLUOROCHEM
Hersteller-Artikelnummer::
023161-1G
Lokale Artikelnummer::
FLUO023161-1G
Beschreibung:
3',5'-Dichlor-2,2,2-trifluoracetophenon
VE:
1 * 1 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(USBIC2096-64F)
Lieferant:
US Biological
Hersteller-Artikelnummer::
C2096-64F
Lokale Artikelnummer::
USBIC2096-64F
Beschreibung:
Anti-CTNNB1 Rabbit polyclonal antibody
VE:
1 * 100 µG
Artikel-Nr:
(LAMA2450-2)
Lieferant:
LAMAPLAST
Hersteller-Artikelnummer::
2450-2
Lokale Artikelnummer::
LAMA2450-2
Beschreibung:
PP, white.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-11604R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11604R-HRP
Lokale Artikelnummer::
BOSSBS-11604R-HRP
Beschreibung:
Na+/Cl- dependent neurotransmitter transporters are a superfamily of transmembrane proteins that contain 12 membrane spanning regions (1). Specifically, the highly hydrophobic Na+/Cl- dependent glycine transporters (GlyT) are crucial for the termination of neurotransmission at glycinergic synapses (2,3). Two different GlyT genes encode GlyT2 and GlyT1, which exists as two isoforms produced by alternative splicing of the same gene located on human chromosome 1p31.3 (3,4). The GlyT1 gene may be an early marker of neural development and encodes glia-specific transporter proteins (3). Although GlyT1 and GlyT2 are both expressed in the brain and spinal cord, each shows a unique pattern of expression (3,5,6). GlyT1 is found only in the white matter of the CNS, whereas GlyT2 is found in the gray matter of the CNS as well as in macrophages and mast cells in peripheral tissues (3,5). The anatomic distribution of GlyT2 mRNA suggests that glycine may act as a supraspinal neurotransmitter and may function as a chemical messenger outside the CNS (5).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12883R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12883R-A488
Lokale Artikelnummer::
BOSSBS-12883R-A488
Beschreibung:
The breast cancer susceptibility gene (BRCA1) localizes to chromosome 17q. Mutations within this gene account for approximately 45% of families with high incidence of breast cancer and at least 80% of families with increased incidence of both early-onset breast cancer and ovarian cancer. A second breast cancer susceptibility gene, BRCA2, located on chromosome 13q12-13, also confers a high incidence of breast cancer, but unlike BRCA1, BRCA2 does not confer a substantially elevated risk of ovarian cancer. The BRCA2-Associated Factor 35 (BRAF35) protein forms a complex with BRCA2, which associates with condensed chromatin during histone H3 phosphorylation. BRAF35 expression levels are highest in proliferating tissues and parallel BRCA2 expression patterns. The structure of BRAF35 includes a kinesin-like coiled coil domain and a nonspecific DNA binding HMG domain. The chromatin localization of BRAF35 and antibody microinjection studies indicate a role for the BRAF35/BRCA2 complex in cell cycle regulation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11604R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11604R-A350
Lokale Artikelnummer::
BOSSBS-11604R-A350
Beschreibung:
Na+/Cl- dependent neurotransmitter transporters are a superfamily of transmembrane proteins that contain 12 membrane spanning regions (1). Specifically, the highly hydrophobic Na+/Cl- dependent glycine transporters (GlyT) are crucial for the termination of neurotransmission at glycinergic synapses (2,3). Two different GlyT genes encode GlyT2 and GlyT1, which exists as two isoforms produced by alternative splicing of the same gene located on human chromosome 1p31.3 (3,4). The GlyT1 gene may be an early marker of neural development and encodes glia-specific transporter proteins (3). Although GlyT1 and GlyT2 are both expressed in the brain and spinal cord, each shows a unique pattern of expression (3,5,6). GlyT1 is found only in the white matter of the CNS, whereas GlyT2 is found in the gray matter of the CNS as well as in macrophages and mast cells in peripheral tissues (3,5). The anatomic distribution of GlyT2 mRNA suggests that glycine may act as a supraspinal neurotransmitter and may function as a chemical messenger outside the CNS (5).
VE:
1 * 100 µl
Artikel-Nr:
(LAUDRKJ112)
Lieferant:
LAUDA
Hersteller-Artikelnummer::
RKJ112
Lokale Artikelnummer::
LAUDRKJ112
Beschreibung:
Polymer tubing, EPDM or silicone
VE:
1 * 1 m
Artikel-Nr:
(BLEG104445)
Lieferant:
BIOLEGEND INC
Hersteller-Artikelnummer::
104445
Lokale Artikelnummer::
BLEG104445
Beschreibung:
Anti-SELL Rat Monoclonal Antibody (Brilliant Violet® 711) [clone: MEL-14]
VE:
1 * 50 µG
This is a MarketSource item. Additional charges may apply
Lieferant:
Sigma-Aldrich
Beschreibung:
Spermidin, Sigma-Aldrich®
Lieferant:
KARTELL
Beschreibung:
PP, durchscheinend.
Artikel-Nr:
(BOSSBS-7116R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7116R-CY5
Lokale Artikelnummer::
BOSSBS-7116R-CY5
Beschreibung:
Ro autoantigens are of clinical significance because directed against them are found in most patients with primary Sjqgren syndrome, subacute cutaneous lupus erythematosus (SLE), neonatal lupus erythematosus, ANA-negative lupus erythematosus, and systemic lupus erythematosus-like disease secondary to homozygous C2 or C4 complement deficiency (1). Ro/SSA is a ribonucleoprotein that binds to auto in 35 to 50% of patients with SLE and in up to 97% of patients with Sjqgren syndrome (2). The Ro/SSA particle consists of a single immunoreactive protein noncovalently bound with one of four small RNA molecules (2). Most anti-Ro/SSA-positive sera detect not only the main protein, but also a smaller Ro/SSA protein (2). The genes which encode the smaller and larger proteins map to human chromosomes 11p15.5 and 1q31, respectively (3?). La/SSB is an autoimmune RNA-binding protein that plays a role in the transcription of RNA polymerase III was originally defined by its reactivity with auto from patients with Sjé°ƒren syndrome and SLE (6).
VE:
1 * 100 µl
Artikel-Nr:
(265005-100)
Lieferant:
Merck Millipore (Calbiochem)
Hersteller-Artikelnummer::
265005-100
Lokale Artikelnummer::
CALB265005-100
Beschreibung:
Dexamethason, Millipore®
VE:
1 * 100 mg
Lieferant:
Sigma-Aldrich
Beschreibung:
2,6-Dimethoxy-p-kresol, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-9681R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9681R-FITC
Lokale Artikelnummer::
BOSSBS-9681R-FITC
Beschreibung:
C19orf45 is a 505 amino acid protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and 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 Fcα 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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9678R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9678R-A488
Lokale Artikelnummer::
BOSSBS-9678R-A488
Beschreibung:
C19orf21 is a 679 amino acid protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and 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 Fcα 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.
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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