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3-(3-Methoxyphenoxy)butan-2-one
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3-(3-Methoxyphenoxy)butan-2-one
Artikel-Nr:
(BOSSBS-4819R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4819R-A488
Lokale Artikelnummer::
BOSSBS-4819R-A488
Beschreibung:
Protein tyrosine-protein phosphatase required for T-cell activation through the antigen receptor. Acts as a positive regulator of T-cell coactivation upon binding to DPP4. The first PTPase domain has enzymatic activity, while the second one seems to affect the substrate specificity of the first one. Upon T-cell activation, recruits and dephosphorylates SKAP1 and FYN (By similarity). Dephosphorylates LYN, and thereby modulates LYN activity (By similarity).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2617R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2617R-A555
Lokale Artikelnummer::
BOSSBS-2617R-A555
Beschreibung:
Plays a role in the export of proteins that lack a signal peptide and are secreted by an alternative pathway. Binds two calcium ions per subunit. Binds one copper ion. Binding of one copper ion does not interfere with calcium binding. Required for the copper-dependent stress-induced export of IL1A and FGF1. The calcium-free protein binds to lipid vesicles containing phosphatidylserine, but not to vesicles containing phosphatidylcholine (By similarity).
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD108756-10G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD108756-10G
Lokale Artikelnummer::
BLDPBD108756-10G
Beschreibung:
6-Chlor-2-hydroxypyridin 98%
VE:
1 * 10 g
Artikel-Nr:
(BOSSBS-1890R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1890R-A555
Lokale Artikelnummer::
BOSSBS-1890R-A555
Beschreibung:
Voltage-gated sodium channels are transmembrane glycoprotein complexes composed of a large alpha subunit with 24 transmembrane domains and one or more regulatory beta subunits. They are responsible for the generation and propagation of action potentials in neurons and muscle. This gene encodes one member of the sodium channel alpha subunit gene family. It is heterogeneously expressed in the brain, and mutations in this gene have been linked to several seizure disorders. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11975R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11975R-A555
Lokale Artikelnummer::
BOSSBS-11975R-A555
Beschreibung:
CacyBP is a 228 amino acid protein encoded by the human gene CACYBP. CacyBP is primarily a nuclear protein that contains one CS domain and one SGS domain. CacyBP is believed to be involved in calcium-dependent ubiquitination and subsequent proteosomal degradation of target proteins. It most likely serves as a molecular bridge in ubiquitin E3 complexes. It also participates in the ubiquitin-mediated degradation of b-catenin. CacyBP is thought to be a potential inhibitor of cell growth and invasion in the gastric cancer cell through its effects on b-catenin protein expression and transcriptional activation of TCF/LEF.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-1890R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1890R-FITC
Lokale Artikelnummer::
BOSSBS-1890R-FITC
Beschreibung:
Voltage-gated sodium channels are transmembrane glycoprotein complexes composed of a large alpha subunit with 24 transmembrane domains and one or more regulatory beta subunits. They are responsible for the generation and propagation of action potentials in neurons and muscle. This gene encodes one member of the sodium channel alpha subunit gene family. It is heterogeneously expressed in the brain, and mutations in this gene have been linked to several seizure disorders. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4'-Amino-2'-hydroxyacetophenon
Artikel-Nr:
(BOSSBS-17166R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-17166R-A680
Lokale Artikelnummer::
BOSSBS-17166R-A680
Beschreibung:
This gene encodes a member of the pterin-dependent aromatic acid hydroxylase family. The encoded protein catalyses the first and rate limiting step in the biosynthesis of serotonin, an important hormone and neurotransmitter. The human genome contains two related tryptophan hydroxylases, one on chromosome 11p15-p14 and one on chromosome 12q21. This gene is expressed predominantly in the brain stem. Mutations in this gene may be associated with psychiatric diseases such as bipolar affective disorder and major depression.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
4'-Brom-4-chlorbutyrophenon ≥98%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
(R)-(+)-4-Benzyl-2-oxazolidinon
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3',5'-Dimethoxy-4'-hydroxyacetophenon 99%
Artikel-Nr:
(BLDPBD33876-10G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD33876-10G
Lokale Artikelnummer::
BLDPBD33876-10G
Beschreibung:
9-Boc-3-oxo-9-azabicyclo[3.3.1]nonane 97%
VE:
1 * 10 g
Lieferant:
Alfa Aesar
Beschreibung:
3-Hydroxy-5-methylisoxazol ≥97%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
8-Chlor-2-methyl-4-chinazolon
Lieferant:
Avantor
Beschreibung:
Aceton 99,5-100,5% (durch Trockensubstanz) NF, Multikompendial, J.T.Baker®
Artikel-Nr:
(BOSSBS-9380R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9380R-A350
Lokale Artikelnummer::
BOSSBS-9380R-A350
Beschreibung:
Midline-1 (Tripartite motif-containing protein 18, Putative transcription factor XPRF, RING finger protein 59) is a 667 amino acid protein encoded by the human gene MID1. Midline-1 belongs to the TRIM/RBCC family and contains two B box-type zinc fingers, one B30.2/SPRY domain, one COS domain, one fibronectin type-III domain and one RING-type zinc finger. Midline-1 is believed to have E3 ubiquitin ligase activity which targets the catalytic subunit of protein phosphatase 2 for degradation. It is a cytoplasmic protein found as a homodimer or heterodimer with Midline-2. It also interacts with IGBP1 (Lymphocyte signaling protein A4). Defects in MID1 are the cause of Opitz syndrome type I (OS-I). OS-I is an X-linked recessive disorder characterized by hypertelorism, genital-urinary defects such as hypospadias in males and splayed labia in females, lip-palate-laryngotracheal clefts, imperforate anus, developmental delay and congenital heart defects. OS-I mutations produce proteins with a decreased affinity for microtubules.
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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