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Bis(3-fluorphenyl)disulfid
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Bis(3-fluorphenyl)disulfid
Artikel-Nr:
(CHMPFL13187.POR)
Lieferant:
CHEMPUR
Hersteller-Artikelnummer::
FL13187.POR
Lokale Artikelnummer::
CHMPFL13187.POR
Beschreibung:
2-Fluorphenylacetat
VE:
1 * 1 ST
Artikel-Nr:
(FLUO020882-1G)
Lieferant:
FLUOROCHEM
Hersteller-Artikelnummer::
020882-1G
Lokale Artikelnummer::
FLUO020882-1G
Beschreibung:
(3-Fluorphenyl)methansulfonsäurechlorid
VE:
1 * 1 g
 This is a MarketSource item. Additional charges may apply
Lieferant:
Biosensis
Beschreibung:
MC192-saporin is an antibody conjugate comprising of the monoclonal antibody MC192 against rat p75NTR, the nerve growth factor receptor, chemically conjugated via a reducible disulfide bridge to the ribosome-inactivating protein saporin, purified from saponaria officinalis.
Artikel-Nr:
(BOSSBS-11337R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11337R-CY3
Lokale Artikelnummer::
BOSSBS-11337R-CY3
Beschreibung:
C1q, a subcomponent of the classical complement pathway, is composed of nine subunits that mediate classical complement activation and thereby play an important role in the immune response. Six of these subunits are disulfide-linked dimers of chains A and B, while three of these subunits, designated C1q-A through C1q-C, are disulfide-linked dimers of chain C. The presence of receptors for C1q on effector cells modulates its activity, which may be antibody-dependent or independent. Macrophages are the primary source of C1q, while anti-inflammatory drugs as well as cytokines differentially regulate expression of the mRNA, as well as the protein. However, its ability to modulate the interaction of platelets with collagen and immune complexes suggests C1q influences homeostasis as well as other immune activities, and perhaps thrombotic complications resulting from immune injury. Defects in C1q-A, C1q-B and C1q-C cause inactivation of the classical pathway, leading to a rare genetic disorder characterized by lupus-like symptoms.
VE:
1 * 100 µl
Lieferant:
FLUOROCHEM
Beschreibung:
4-Brom-2-fluorzimtsäure
Artikel-Nr:
(BOSSBS-11337R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11337R-CY7
Lokale Artikelnummer::
BOSSBS-11337R-CY7
Beschreibung:
C1q, a subcomponent of the classical complement pathway, is composed of nine subunits that mediate classical complement activation and thereby play an important role in the immune response. Six of these subunits are disulfide-linked dimers of chains A and B, while three of these subunits, designated C1q-A through C1q-C, are disulfide-linked dimers of chain C. The presence of receptors for C1q on effector cells modulates its activity, which may be antibody-dependent or independent. Macrophages are the primary source of C1q, while anti-inflammatory drugs as well as cytokines differentially regulate expression of the mRNA, as well as the protein. However, its ability to modulate the interaction of platelets with collagen and immune complexes suggests C1q influences homeostasis as well as other immune activities, and perhaps thrombotic complications resulting from immune injury. Defects in C1q-A, C1q-B and C1q-C cause inactivation of the classical pathway, leading to a rare genetic disorder characterized by lupus-like symptoms.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13162R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13162R-A647
Lokale Artikelnummer::
BOSSBS-13162R-A647
Beschreibung:
Ficolin B is the designation in mouse and rat of a protein also known as L-ficolin, ficolin-2, collagen/fibrinogen domain-containing protein 2, serum lectin p35, EBP-37 or hucolin. Ficolin B is a 313 amino acid member of the ficolin lectin family. It is a secreted innate immunity pattern recognition molecule expressed in liver and plasma that forms a disulfide-linked homopolymer. This extensive N-terminal disulfide bridge formation can lead to a functional dodecamer polypeptide. Ficolin B binds to DNA ligands expressed by late apoptotic and necrotic cells to increase attachment and engulfment. Variation in ficolin B concentrations amongst individuals is associated with polymorphisms in the promoter and structural portion of the FCN2 gene. In patients with Behé´t's disease (BD), there exists a significant difference in allele frequency for FCN2 gene single nucleotide polymorphisms (SNPs) within the -557 and -64 promoter sites within HLA-B51 positive and HLA-B51 negative subgroups.
VE:
1 * 100 µl
Artikel-Nr:
(CHMPFL13231.POR)
Lieferant:
CHEMPUR
Hersteller-Artikelnummer::
FL13231.POR
Lokale Artikelnummer::
CHMPFL13231.POR
Beschreibung:
3-Brom-5-fluorzimtsäure
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-1276R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1276R-A680
Lokale Artikelnummer::
BOSSBS-1276R-A680
Beschreibung:
This gene encodes an endoplasmic reticulum co-chaperone which is part of the endoplasmic reticulum-associated degradation complex involved in recognizing and degrading misfolded proteins. The encoded protein reduces incorrect disulfide bonds in misfolded glycoproteins. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6447R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6447R-HRP
Lokale Artikelnummer::
BOSSBS-6447R-HRP
Beschreibung:
Protamines substitute for histones in the chromatin of sperm during the haploid phase of spermatogenesis. They compact sperm DNA into a highly condensed, stable and inactive complex. Protamines are cross-linked by interchain disulfide bonds around the DNA-helix. Protamines are localised in the nucleus. This protein is found only in the testis and belongs to the protamine P1 family.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
2',4'-Dichlor-5'-fluoracetophenon
Lieferant:
Thermo Scientific
Beschreibung:
3-(2-Chlor-6-fluorphenyl)-5-methyl-4-isoxazolcarbonsäurechlorid
Artikel-Nr:
(BOSSBS-13162R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13162R-A750
Lokale Artikelnummer::
BOSSBS-13162R-A750
Beschreibung:
Ficolin B is the designation in mouse and rat of a protein also known as L-ficolin, ficolin-2, collagen/fibrinogen domain-containing protein 2, serum lectin p35, EBP-37 or hucolin. Ficolin B is a 313 amino acid member of the ficolin lectin family. It is a secreted innate immunity pattern recognition molecule expressed in liver and plasma that forms a disulfide-linked homopolymer. This extensive N-terminal disulfide bridge formation can lead to a functional dodecamer polypeptide. Ficolin B binds to DNA ligands expressed by late apoptotic and necrotic cells to increase attachment and engulfment. Variation in ficolin B concentrations amongst individuals is associated with polymorphisms in the promoter and structural portion of the FCN2 gene. In patients with Beht's disease (BD), there exists a significant difference in allele frequency for FCN2 gene single nucleotide polymorphisms (SNPs) within the -557 and -64 promoter sites within HLA-B51 positive and HLA-B51 negative subgroups.
VE:
1 * 100 µl
Artikel-Nr:
(COBBHC-2398-1G)
Lieferant:
COMBI-BLOCKS
Hersteller-Artikelnummer::
HC-2398-1G
Lokale Artikelnummer::
COBBHC-2398-1G
Beschreibung:
Ethyl-5-amino-4-cyan-1-(2-fluorphenyl)-1H-pyrazol-3-carboxylat
VE:
1 * 1 g
This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(COBBHC-2397-1G)
Lieferant:
COMBI-BLOCKS
Hersteller-Artikelnummer::
HC-2397-1G
Lokale Artikelnummer::
COBBHC-2397-1G
Beschreibung:
Ethyl-5-amino-4-cyan-1-(3-fluorphenyl)-1H-pyrazol-3-carboxylat
VE:
1 * 1 g
This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BOSSBS-9502R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9502R-A350
Lokale Artikelnummer::
BOSSBS-9502R-A350
Beschreibung:
This gene encodes coagulation factor XI of the blood coagulation cascade. This protein is present in plasma as a zymogen, which is a unique plasma coagulation enzyme because it exists as a homodimer consisting of two identical polypeptide chains linked by disulfide bonds. During activation of the plasma factor XI, an internal peptide bond is cleaved by factor XIIa (or XII) in each of the two chains, resulting in activated factor XIa, a serine protease composed of two heavy and two light chains held together by disulfide bonds. This activated plasma factor XI triggers the middle phase of the intrisic pathway of blood coagulation by activating factor IX. Defects in this factor lead to Rosenthal syndrome, a blood coagulation abnormality. [provided by RefSeq, Jul 2008].
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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