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3,4-(Ethylendioxy)benzylamin
Lieferant:
Tonbo Biosciences
Beschreibung:
The 53-6.7 antibody reacts with the 32-34 kDa alpha subunit of mouse CD8, known as CD8a or CD8 alpha. CD8a can form a homodimer (CD8 alpha-alpha), but is more commonly expressed as a heterodimer with a second chain known as CD8b or CD8 beta. CD8 acts as a co-receptor in antigen recognition and subsequent T cell activation that is initiated upon binding of the T cell receptor (TCR) to antigen-bearing MHC Class I molecules. The cytoplasmic domains of CD8 provide binding sites for the tyrosine kinase lck, facilitating intracellular signaling events that lead to T cell activation, development, and cytotoxic effector functions. CD8+ cytotoxic T cells (CTLs) play an important role in inducing cell death of tumor cells, as well as cells infected by virus, bacteria or parasites.
Lieferant:
Tonbo Biosciences
Beschreibung:
The Hit8a antibody is specific for the 32-34 kDa alpha chain of human CD8, known as CD8a or CD8 alpha. CD8a can form a homodimer (CD8 alpha-alpha), but is more commonly expressed as a heterodimer with a second chain known as CD8b or CD8 beta. CD8 acts as a co-receptor for antigen recognition and subsequent T cell activation that is initiated upon binding of the T cell receptor (TCR) to antigen-bearing MHC Class I molecules. The cytoplasmic domains of CD8 provide binding sites for the tyrosine kinase lck, facilitating intracellular signaling events that lead to T cell activation, development, and cytotoxic effector functions. CD8+ cytotoxic T cells (CTLs) play an important role in inducing cell death of tumor cells, as well as cells infected by virus, bacteria or parasites.
Artikel-Nr:
(EHERL20014900IO)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
L20014900IO
Lokale Artikelnummer::
EHERL20014900IO
Beschreibung:
Organic Standard, 2,2',3,4',5',6-Hexachlorbiphenyl (PCB Nr. 149) 10 µg/ml in Isooctan, Packung: Glasflasche
VE:
1 * 10 mL
Artikel-Nr:
(EHERL20009000IO)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
L20009000IO
Lokale Artikelnummer::
EHERL20009000IO
Beschreibung:
Organic Standard, 2,2',3,4',5-Pentachlorbiphenyl (PCB Nr. 90) 10 µg/ml in Isooctan, Packung: Glasflasche
VE:
1 * 10 mL
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
D(+)-Raffinose Pentahydrat
Lieferant:
Tonbo Biosciences
Beschreibung:
The RPA-T8 antibody is specific for the 32-34 kDa alpha chain of human CD8, known as CD8a or CD8 alpha. CD8a can form a homodimer (CD8 alpha-alpha), but is more commonly expressed as a heterodimer with a second chain known as CD8b or CD8 beta. CD8 acts as a co-receptor for antigen recognition and subsequent T cell activation that is initiated upon binding of the T cell receptor (TCR) to antigen-bearing MHC Class I molecules. The cytoplasmic domains of CD8 provide binding sites for the tyrosine kinase lck, facilitating intracellular signaling events that lead to T cell activation, development, and cytotoxic effector functions. CD8+ cytotoxic T cells (CTLs) play an important role in inducing cell death of tumor cells, as well as cells infected by virus, bacteria or parasites.
Artikel-Nr:
(BOSSBS-4278R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4278R-A488
Lokale Artikelnummer::
BOSSBS-4278R-A488
Beschreibung:
This gene is an ortholog of the Drosophila fat gene, which encodes a tumor suppressor essential for controlling cell proliferation during Drosophila development. The gene product is a member of the cadherin superfamily, a group of integral membrane proteins characterized by the presence of cadherin-type repeats. In addition to containing 34 tandem cadherin-type repeats, the gene product has five epidermal growth factor (EGF)-like repeats and one laminin A-G domain. This gene is expressed at high levels in a number of fetal epithelia. Its product probably functions as an adhesion molecule and/or signaling receptor, and is likely to be important in developmental processes and cell communication. Transcript variants derived from alternative splicing and/or alternative promoter usage exist, but they have not been fully described. [provided by RefSeq].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13642R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13642R-HRP
Lokale Artikelnummer::
BOSSBS-13642R-HRP
Beschreibung:
Many growth factors function by binding receptors with intrinsic tyrosine kinase activity (1,2). Signaling by such receptors involves a series of intermediates characterized by SH2 domains that bind tyrosine phosphorylated receptors by a direct interaction between the SH2 domain and the phosphotyrosine-containing receptor sequences (3,4). GRB7, a SH2 domain protein, has a single SH2 domain at its C-terminal, a central region with similarity to Ras GAP and a proline-rich N-terminus (5,6). GRB7 maps to the region on mouse chromosome 11 containing the Neu gene (6). This region of mouse chromosome 11 is syntenic to an area of human chromosome 17q that is frequently amplified in breast cancer (6,7). Moreover, GRB7 is amplified and over-expressed in breast cancer and is found in a complex with Neu gp185 (6).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15175R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15175R-A350
Lokale Artikelnummer::
BOSSBS-15175R-A350
Beschreibung:
C3orf34 (chromosome 3 open reading frame 34), also known as MGC14126, is a 163 amino acid protein encoded by a gene that maps to human chromosome 3q29. Chromosome 3 is made up of approximately 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth disease are a few of the numerous genetic diseases associated with chromosome 3.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11318R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11318R-CY7
Lokale Artikelnummer::
BOSSBS-11318R-CY7
Beschreibung:
The human ataxin-7 gene, also known as spinocerebellar ataxia 7 or SCA7, maps to chromosome 3p13-p12, has a 2,727-bp open reading frame, and encodes a 892 amino acid protein containing a nuclear localization signal and a polyglutamine tract (1,2). SCA7 is an autosomal dominant neurodegenerative disorder characterized by ataxia and selective neuronal cell loss caused by the expansion of a translated CAG repeat encoding a polyglutamine tract in ataxin-7, which is the SCA7 gene product (3,4). Ataxin-7 is expressed within neurons both affected and unaffected in SCA7 pathology with subcellular localization being variable depending upon the neuronal subtype (5). Polyglutamine expanded in ataxin-7 may carry out its pathogenic effects in the nucleus by altering the matrix-associated nuclear structure and/or by disrupting nucleolar function (6).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9500R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9500R-CY5
Lokale Artikelnummer::
BOSSBS-9500R-CY5
Beschreibung:
Hemostasis following tissue injury involves the deployment of essential plasma procoagulants (prothrombin, and factors X, IX, V, and VIII), which are involved in a blood coagulation cascade that leads to the formation of insoluble fibrin clots and the promotion of platelet aggregation (1-3). Coagulation factor IX (plasma thromboplastic component, F9, F.IX, HEMB) is a vitamin K-dependent, single chain serine protease that is synthesized in the liver and circulates as an inactive precursor (3,4). Factor XIa mediated proteolytic cleavage of factor IX generates factor IXa, an active serine protease composed of a 145 amino acid light chain and a 236 amino acid catalytic heavy chain, linked through disulfide bonds (5). Genetic alterations at the Factor IX locus such as point mutations, insertions and deletions, can lead to hemophilia B, also known as Christmas disease (6).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11318R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11318R-CY5
Lokale Artikelnummer::
BOSSBS-11318R-CY5
Beschreibung:
The human ataxin-7 gene, also known as spinocerebellar ataxia 7 or SCA7, maps to chromosome 3p13-p12, has a 2,727-bp open reading frame, and encodes a 892 amino acid protein containing a nuclear localization signal and a polyglutamine tract (1,2). SCA7 is an autosomal dominant neurodegenerative disorder characterized by ataxia and selective neuronal cell loss caused by the expansion of a translated CAG repeat encoding a polyglutamine tract in ataxin-7, which is the SCA7 gene product (3,4). Ataxin-7 is expressed within neurons both affected and unaffected in SCA7 pathology with subcellular localization being variable depending upon the neuronal subtype (5). Polyglutamine expanded in ataxin-7 may carry out its pathogenic effects in the nucleus by altering the matrix-associated nuclear structure and/or by disrupting nucleolar function (6).
VE:
1 * 100 µl
Artikel-Nr:
(PROOMM0136.05)
Lieferant:
LGC Standards PROMOCHEM
Hersteller-Artikelnummer::
MM0136.05
Lokale Artikelnummer::
PROOMM0136.05
Beschreibung:
Organic Standard, (4RS)-3-Amino-6-chloro-2-methyl-4-phenyl-3,4-dihydroquinazolin-4-ol
VE:
1 * 50 mg
Lieferant:
Thermo Scientific
Beschreibung:
3',4'-Difluoracetophenon
Artikel-Nr:
(EHERL14640000AL)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
L14640000AL
Lokale Artikelnummer::
EHERL14640000AL
Beschreibung:
Organic Standard, Linuron (N-(3,4-Dichlorphenyl)-N'-methoxy,N'-methylharnstoff) 10 µg/ml in Acetonitril, Packung: Glasflasche
VE:
1 * 10 mL
Artikel-Nr:
(MOLEM43971872)
Lieferant:
Molekula
Hersteller-Artikelnummer::
M43971872
Lokale Artikelnummer::
MOLEM43971872
Beschreibung:
Veratraldehyd
VE:
1 * 500 g
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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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