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2-Acetamido-3-fluorobenzoic+acid
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2-Acetamido-3-fluorobenzoic+acid
Lieferant:
FLUOROCHEM
Beschreibung:
3,4-Dichlorthiophenol
Lieferant:
Thermo Scientific
Beschreibung:
4-Iod-o-xylol
Lieferant:
Bernd Kraft
Beschreibung:
di-Natriumhydrogenphosphat Dodecahydrat analytisches Reagens
Lieferant:
Sigma-Aldrich
Beschreibung:
tri-Natriumphosphat Dodecahydrat, Sigma-Aldrich®
Lieferant:
Sigma-Aldrich
Beschreibung:
(R)-(-)-2,2-Dimethyl-1,3-dioxolan-4-ylmethanol, Sigma-Aldrich®
Lieferant:
BIOLEGEND INC
Beschreibung:
Anti-Adenomatous polyposis coli (APC) Mouse Monoclonal Antibody [clone: Ali 12-28]
Artikel-Nr:
(USBI132885)
Lieferant:
US Biological
Hersteller-Artikelnummer::
132885
Lokale Artikelnummer::
USBI132885
Beschreibung:
Anti-RUFY1 Rabbit Polyclonal Antibody
VE:
1 * 100 µG
Lieferant:
Sigma-Aldrich
Beschreibung:
(S)-(+)-Epichlorhydrin, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-11769R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11769R-A555
Lokale Artikelnummer::
BOSSBS-11769R-A555
Beschreibung:
The majority of mitochondrial-directed proteins are encoded by the nuclear genome and are transported to the mitochondria via regulated processes involving the mitochondrial Tom and Tim proteins (1). The mitochondrial Tim protein family is comprised of a large group of evolutionarily conserved proteins that are found in most eukaryotes (1,2). Import of nuclear-encoded precursor proteins into and across the mitochondrial inner membrane is mediated by two distinct complexes, the Tim23 complex and the Tim22 complex, which differ in their substrate specificity (1). Defects in Tim proteins are implicated in several neuro-degenerative diseases, suggesting important roles for Tim proteins in development and health (3,4). Tim8A and Tim8B, which map to human chromosomes Xq22.1 and 11q23.1-q23.2, respectively, are conserved proteins of the mitochondrial intermembrane space, which are organized in hetero-oligomeric complex with Tim13 (5,6,7). Tim8A is highly expressed in fetal and adult brain (5). Tim8A is mutated in deafness dystonia syndrome, a novel type of disease that causes severe neurological defects, thought to be caused by a defective mitochondrial protein transport system (5,8).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11512R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11512R-A647
Lokale Artikelnummer::
BOSSBS-11512R-A647
Beschreibung:
Bardet-Biedl syndrome (BBS) is a pleiotropic genetic disorder characterized by obesity, photoreceptor degeneration, polydactyly, hypogenitalism, renal abnormalities, and developmental delay. Other associated clinical findings in BBS patients include diabetes, hypertension, and congenital heart defects. BBS genes map to multiple loci and encode fourteen proteins, BBS1-BBS14. Many BBS genes encode basal body or cilia proteins, suggesting that BBS is a ciliary dysfunction disorder. BBS10 (Bardet-Biedl syndrome 10), also known as chromosome 12 open reading fame 58, C12orf58 or FLJ23560, is a novel 723 amino acid protein belonging to the TCP-1 chaperonin family. BBS10 localizes to the basal body of primary cilium and assists in protein folding upon ATP hydrolysis. Inhibition of BBS10 has been found to impair ciliogenesis, activate the glycogen synthase kinase 3 pathway and cause peroxisome proliferator-activated receptor nuclear accumulation. The gene encoding BBS10 contains two exons and maps to human chromosome 12q21.2.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11769R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11769R-FITC
Lokale Artikelnummer::
BOSSBS-11769R-FITC
Beschreibung:
The majority of mitochondrial-directed proteins are encoded by the nuclear genome and are transported to the mitochondria via regulated processes involving the mitochondrial Tom and Tim proteins (1). The mitochondrial Tim protein family is comprised of a large group of evolutionarily conserved proteins that are found in most eukaryotes (1,2). Import of nuclear-encoded precursor proteins into and across the mitochondrial inner membrane is mediated by two distinct complexes, the Tim23 complex and the Tim22 complex, which differ in their substrate specificity (1). Defects in Tim proteins are implicated in several neuro-degenerative diseases, suggesting important roles for Tim proteins in development and health (3,4). Tim8A and Tim8B, which map to human chromosomes Xq22.1 and 11q23.1-q23.2, respectively, are conserved proteins of the mitochondrial intermembrane space, which are organized in hetero-oligomeric complex with Tim13 (5,6,7). Tim8A is highly expressed in fetal and adult brain (5). Tim8A is mutated in deafness dystonia syndrome, a novel type of disease that causes severe neurological defects, thought to be caused by a defective mitochondrial protein transport system (5,8).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11461R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11461R-A555
Lokale Artikelnummer::
BOSSBS-11461R-A555
Beschreibung:
Growth/differentiation factors (GDFs) are members of the TGF superfamily (1,2). Members of the TGF superfamily are involved in embryonic development and adult tissue homeostasis (1). GDF-1 expression is almost exclusively restricted to the central nervous system and mediates cell differentiation events during embryonic development (3). Neither GDF-3 (Vgr-2) nor GDF-9 contains the conserved cysteine residue which is found in most other TGF superfamily members. GDF-3 is detectable in bone marrow, spleen, thymus and adipose tissue, whereas GDF-9 has only been detected in ovary (4). GDF-5 (also designated CDMP-1) has been shown to induce activation of plasminogen activator, thereby inducing angiogenesis. It is predominantly expressed in long bones during fetal embryonic development and is involved in bone formation. (5). GDF-5 mutations have been identified in mice with the mutation brachypodism (bp), a mutation which affects the length and number of bones in limbs (6). GDF-6 and GDF-7 are closely related to GDF-5 (6). GDF-8 has been shown to be a negative regulator of skeletal muscle mass (1).
VE:
1 * 100 µl
Artikel-Nr:
(MOLEM68359886)
Lieferant:
Molekula
Hersteller-Artikelnummer::
M68359886
Lokale Artikelnummer::
MOLEM68359886
Beschreibung:
(±)-α-Liponsäure
VE:
1 * 25 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BLEG572109)
Lieferant:
BIOLEGEND INC
Hersteller-Artikelnummer::
572109
Lokale Artikelnummer::
BLEG572109
Beschreibung:
ELISA Standard four pack contains four vials of recombinant human IL-12/IL-23 (p40) at >5 ng per vial. Recommended for ELISA application only. Standards are calibrated against a BioLegend Master Calibrator.
VE:
1 * 1 Pack.
This is a MarketSource item. Additional charges may apply
Lieferant:
BOCHEM
Beschreibung:
Galvanised steel.
Artikel-Nr:
(736-0198)
Lieferant:
THERMO MATRIX TECHNOLOGIES
Hersteller-Artikelnummer::
AB-1127
Lokale Artikelnummer::
MATRAB-1127
Beschreibung:
PP. The square well geometry of this 96-well plate makes it ideal for bacterial growth applications.
VE:
1 * 50 ST
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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