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(4-Chlor-3-(trifluormethyl)phenyl)essigsäure
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(4-Chlor-3-(trifluormethyl)phenyl)essigsäure
Artikel-Nr:
(BOSSBS-11363R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11363R-CY5
Lokale Artikelnummer::
BOSSBS-11363R-CY5
Beschreibung:
SNAP 29 is a 258 amino acid protein that localizes to the membrane and the cytoplasm, as well as to the cell junction, and contains one t-SNARE coiled-coil homology domain. Expressed in liver, heart, brain, kidney, placenta, lung, spleen, pancreas and skeletal muscle, SNAP 29 binds tightly to Syntaxins and, via this binding, is involved in membrane trafficking events. Defects in the gene encoding SNAP 29 are the cause of CEDNIK syndrome, a neurocutaneous syndrome that is associated with cerebral dysgenesis, neuropathy, ichthyosis and palmoplantar keratoderma. The gene encoding SNAP 29 maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9115R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9115R-CY7
Lokale Artikelnummer::
BOSSBS-9115R-CY7
Beschreibung:
Unknown. Candidate gene encoding tumor antigens.Members of the BAGE gene family encode antigens that are recognized by cytotoxic T lymphocytes and are also known as CT (cancer/testis) antigens. Generated by juxtacentromeric shuffling of the MLL3 gene, the ancestral BAGE gene was expanded by acrocentric exchanges and/or juxtacentromeric movements.Generally, BAGE proteins are silent in all normal tissues with the exception of testis. BAGE2 and BAGE 3 (B melanoma antigen 2 and 3, respectively), also known as Cancer/testis antigen 2.2 and 2.3 (respectively), are 109 amino acid secreted proteins that are expressed in 22% of melanomas, lung and bladder carcinomas, and are also expressed in normal testis tissue. Like the genes encoding MAGE proteins, BAGE genes are most likely silenced by DNA methylation and/or chromatin compaction in normal tissues other than testis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11363R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11363R-CY3
Lokale Artikelnummer::
BOSSBS-11363R-CY3
Beschreibung:
SNAP 29 is a 258 amino acid protein that localizes to the membrane and the cytoplasm, as well as to the cell junction, and contains one t-SNARE coiled-coil homology domain. Expressed in liver, heart, brain, kidney, placenta, lung, spleen, pancreas and skeletal muscle, SNAP 29 binds tightly to Syntaxins and, via this binding, is involved in membrane trafficking events. Defects in the gene encoding SNAP 29 are the cause of CEDNIK syndrome, a neurocutaneous syndrome that is associated with cerebral dysgenesis, neuropathy, ichthyosis and palmoplantar keratoderma. The gene encoding SNAP 29 maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
Silber hart ≥99,998% (Metall-Basis), Folie, Premion®, hart, Dicke 0.025 mm (0.001 in)
Artikel-Nr:
(BOSSBS-11363R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11363R-FITC
Lokale Artikelnummer::
BOSSBS-11363R-FITC
Beschreibung:
SNAP 29 is a 258 amino acid protein that localizes to the membrane and the cytoplasm, as well as to the cell junction, and contains one t-SNARE coiled-coil homology domain. Expressed in liver, heart, brain, kidney, placenta, lung, spleen, pancreas and skeletal muscle, SNAP 29 binds tightly to Syntaxins and, via this binding, is involved in membrane trafficking events. Defects in the gene encoding SNAP 29 are the cause of CEDNIK syndrome, a neurocutaneous syndrome that is associated with cerebral dysgenesis, neuropathy, ichthyosis and palmoplantar keratoderma. The gene encoding SNAP 29 maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9261R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9261R-FITC
Lokale Artikelnummer::
BOSSBS-9261R-FITC
Beschreibung:
The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in the ubiquitination pathway of protein degradation. RNF185 (ring finger protein 185), also known as FLJ38628, is a 192 amino acid multi-pass membrane protein containing one RING-type zinc finger. Two RNF185 isoforms exist as a result of alternative splicing, and the gene encoding RNF185 maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11363R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11363R-A647
Lokale Artikelnummer::
BOSSBS-11363R-A647
Beschreibung:
SNAP 29 is a 258 amino acid protein that localizes to the membrane and the cytoplasm, as well as to the cell junction, and contains one t-SNARE coiled-coil homology domain. Expressed in liver, heart, brain, kidney, placenta, lung, spleen, pancreas and skeletal muscle, SNAP 29 binds tightly to Syntaxins and, via this binding, is involved in membrane trafficking events. Defects in the gene encoding SNAP 29 are the cause of CEDNIK syndrome, a neurocutaneous syndrome that is associated with cerebral dysgenesis, neuropathy, ichthyosis and palmoplantar keratoderma. The gene encoding SNAP 29 maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
Digalliumtrisulfid ≥99,999% (Metall-Basis)
Lieferant:
Alfa Aesar
Beschreibung:
4,5-Dichlor-3(2H)-pyridazinon ≥98%
Artikel-Nr:
(BLDPBD129758-500G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD129758-500G
Lokale Artikelnummer::
BLDPBD129758-500G
Beschreibung:
EDTA Trikaliumsalz 98+%
VE:
1 * 500 g
Lieferant:
Avantor Fluid Handling
Beschreibung:
Erhaltung der Probenreinheit.
Artikel-Nr:
(ACRO412250250)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
412250250
Lokale Artikelnummer::
ACRO412250250
Beschreibung:
Imidazol-4,5-dicarbonsäure 99%
VE:
1 * 25 g
Lieferant:
Cayman Chemical
Beschreibung:
Calcein-AM ist ein zelldurchdringender Farbstoff, der nach dem Transport in lebende Zellen durch intrazelluläre Esterasen abgespalten und in Calcein umgewandelt wird, das die Membran nicht durchdringen kann.
Artikel-Nr:
(BOSSBS-9261R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9261R-A647
Lokale Artikelnummer::
BOSSBS-9261R-A647
Beschreibung:
The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in the ubiquitination pathway of protein degradation. RNF185 (ring finger protein 185), also known as FLJ38628, is a 192 amino acid multi-pass membrane protein containing one RING-type zinc finger. Two RNF185 isoforms exist as a result of alternative splicing, and the gene encoding RNF185 maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia.
VE:
1 * 100 µl
Artikel-Nr:
(UPOWCS00400/44)
Lieferant:
U-Power
Hersteller-Artikelnummer::
CS00400/44
Lokale Artikelnummer::
UPOWCS00400/44
Beschreibung:
Gefertigt aus weichem PU.
VE:
1 * 1 PAAR
Artikel-Nr:
(BLDPBD20227-250MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD20227-250MG
Lokale Artikelnummer::
BLDPBD20227-250MG
Beschreibung:
9,9-Dimethylfluorene-2,7-diboronic acid bis(pinacol) ester 97%
VE:
1 * 250 mg
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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