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Benzoic+acid-acyl-\\u03B2-D-glucuronide
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Benzoic+acid-acyl-\\u03B2-D-glucuronide
Artikel-Nr:
(BOSSBS-15174R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15174R-FITC
Lokale Artikelnummer::
BOSSBS-15174R-FITC
Beschreibung:
C3orf32 (chromosome 3 open reading frame 32), also known as fls485, is a 353 amino acid protein encoded by a gene that maps to human chromosome 3p26.1. 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:
(APOSOR7183-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR7183-5G
Lokale Artikelnummer::
APOSOR7183-5G
Beschreibung:
2-Chlor-5-pyridinboronsäurepinakolester 97%
VE:
1 * 5 g
Lieferant:
Tonbo Biosciences
Beschreibung:
The OKT8 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.
Lieferant:
Tonbo Biosciences
Beschreibung:
The OKT8 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.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-{[3-Chloro-5-(trifluoromethyl)-2-pyridinyl]sulphanyl}-1H-1,2,4-triazol-5-amine
Artikel-Nr:
(APOSPC8411-500MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC8411-500MG
Lokale Artikelnummer::
APOSPC8411-500MG
Beschreibung:
2-[3-Chloro-5-(trifluoromethyl)-2-pyridinyl]malononitrile
VE:
1 * 500 mg
Artikel-Nr:
(APOSOR346607-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR346607-1G
Lokale Artikelnummer::
APOSOR346607-1G
Beschreibung:
[2-(1-Pyrrolidinyl)-3-pyridinyl]methanol 95+%
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-11944R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11944R-CY7
Lokale Artikelnummer::
BOSSBS-11944R-CY7
Beschreibung:
RILPL2 is a 211 amino acid protein that belongs to the RILPL family. RILPL2 does not regulate lysosomal morphology or distribution. RILPL2 shares 32% and 18% amino acid identity with RILPL1 and RILP, respectively. RILPL2 as a novel interacting partner for the actin-based molecular motor MyoVa, and has a novel role for RILPL2 in controlling neuronal morphogenesis. It has been suggested that there is also a novel role for RILPL2 in the regulation of cellular shape and dendritic-spine morphogenesis, probably via the Rac1-Pak pathway. PCR analysis of human tissues detects highest RILPL2 expression in lung, followed by placenta. Lower expression is detected in liver, kidney, pancreas, heart and brain, but no expression is detected in skeletal muscle. The RILPL2 gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, and maps to human chromosome 12q24.31.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11944R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11944R-CY3
Lokale Artikelnummer::
BOSSBS-11944R-CY3
Beschreibung:
RILPL2 is a 211 amino acid protein that belongs to the RILPL family. RILPL2 does not regulate lysosomal morphology or distribution. RILPL2 shares 32% and 18% amino acid identity with RILPL1 and RILP, respectively. RILPL2 as a novel interacting partner for the actin-based molecular motor MyoVa, and has a novel role for RILPL2 in controlling neuronal morphogenesis. It has been suggested that there is also a novel role for RILPL2 in the regulation of cellular shape and dendritic-spine morphogenesis, probably via the Rac1-Pak pathway. PCR analysis of human tissues detects highest RILPL2 expression in lung, followed by placenta. Lower expression is detected in liver, kidney, pancreas, heart and brain, but no expression is detected in skeletal muscle. The RILPL2 gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, and maps to human chromosome 12q24.31.
VE:
1 * 100 µl
Artikel-Nr:
(APOSOR4386-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR4386-1G
Lokale Artikelnummer::
APOSOR4386-1G
Beschreibung:
5-(3-Pyridinyloxy)-2-furoic acid 97%
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-15174R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15174R-A750
Lokale Artikelnummer::
BOSSBS-15174R-A750
Beschreibung:
C3orf32 (chromosome 3 open reading frame 32), also known as fls485, is a 353 amino acid protein encoded by a gene that maps to human chromosome 3p26.1. 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-15174R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15174R-A647
Lokale Artikelnummer::
BOSSBS-15174R-A647
Beschreibung:
C3orf32 (chromosome 3 open reading frame 32), also known as fls485, is a 353 amino acid protein encoded by a gene that maps to human chromosome 3p26.1. 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-15174R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15174R-A680
Lokale Artikelnummer::
BOSSBS-15174R-A680
Beschreibung:
C3orf32 (chromosome 3 open reading frame 32), also known as fls485, is a 353 amino acid protein encoded by a gene that maps to human chromosome 3p26.1. 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
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Ethyl 3-(chlorosulphonyl)isonicotinate 95%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-[5-(Trifluoromethyl)-2-pyridinyl]benzenecarbaldehyde 95%
Artikel-Nr:
(APOSOR14722-250MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR14722-250MG
Lokale Artikelnummer::
APOSOR14722-250MG
Beschreibung:
3-(2-Pyridyl)-D-alanine
VE:
1 * 250 mg
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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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