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2,2\'-Difluorodiphenyldisulphide
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2,2\'-Difluorodiphenyldisulphide
Artikel-Nr:
(BOSSBS-6606R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6606R-A680
Lokale Artikelnummer::
BOSSBS-6606R-A680
Beschreibung:
There are four members (MRGX1-4) in the human MRGX familly. MRGX1 and MRGX2 receptors stimulate both G Alpha q- and G Alpha i -regulated pathways, while MRGX3 and MRGX4 receptors mainly activate G Alpha q-regulated pathways. G Alpha q proteins are involved in the calcium-signaling pathway downstream of the MRGX receptors. MRGX receptors are unique in that they are expressed in a subset of small dorsal root and trigeminal sensory neurons. Probably involved in the function of nociceptive neurons. May regulate nociceptor function and/or development, including the sensation or modulation of pain. Potently activated by enkephalins including BAM22 (bovine adrenal medulla peptide 22) and BAM (8-22). BAM22 is the most potent compound and evoked a large and dose-dependent release of intracellular calcium in stably transfected cells. G(alpha)q proteins are involved in the calcium-signaling pathway.
VE:
1 * 100 µl
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)
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-(2-Thienyl)-3-[(2,2,2-trifluoroacetyl)amino]propanoic acid
Artikel-Nr:
(APOSOR452057-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR452057-5G
Lokale Artikelnummer::
APOSOR452057-5G
Beschreibung:
(3,4-Dichlorphenoxy)essigsäure 97%
VE:
1 * 5 g
Artikel-Nr:
(APOSBIB1157-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
BIB1157-1G
Lokale Artikelnummer::
APOSBIB1157-1G
Beschreibung:
Big CHAP (N,N-Bis[3-(D-gluconamido)propyl]cholamid)
VE:
1 * 1 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:
(ROCK610-9302)
Lieferant:
Rockland Immunochemicals
Hersteller-Artikelnummer::
610-9302
Lokale Artikelnummer::
ROCK610-9302
Beschreibung:
Antibody Anti-Mouse IgG (H&L) peroxidase conjugated has been assayed against 1.0 µg of Mouse IgG in a standard capture ELISA using ABTS (2,2’-azino-bis-(3-ethylbenthiazoline-6-sulfonic acid)) as a substrate for 30 minutes at room temperature.
VE:
1 * 1 mg
Lieferant:
Alfa Aesar
Beschreibung:
Digalliumtrisulfid ≥99,999% (Metall-Basis)
Lieferant:
Alfa Aesar
Beschreibung:
4,5-Dichlor-3(2H)-pyridazinon ≥98%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Bromo-2-(trifluoromethyl)benzeneboronic acid
Artikel-Nr:
(APOSPC1029-100MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC1029-100MG
Lokale Artikelnummer::
APOSPC1029-100MG
Beschreibung:
5-tert-Butyl-3-(trifluoromethyl)-1H-pyrazole 97%
VE:
1 * 100 mg
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:
(BOSSBS-5592R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5592R-CY5
Lokale Artikelnummer::
BOSSBS-5592R-CY5
Beschreibung:
This gene is the cellular homolog of the Yamaguchi sarcoma virus oncogene. The encoded protein has tyrosine kinase activity and belongs to the src family of proteins. This gene lies in close proximity to thymidylate synthase gene on chromosome 18, and a corresponding pseudogene has been found on chromosome 22. [provided by RefSeq].
VE:
1 * 100 µl
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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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