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RESTEK
Lieferant:
Avantor
Beschreibung:
Aceton, BAKER ANALYZED® HPLC für die HPLC, J.T.Baker®
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
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2,4-Diacetylphloroglucinol 96%
Lieferant:
Thermo Scientific
Beschreibung:
Mifepriston 98%
Artikel-Nr:
(APOSOR89540-50MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR89540-50MG
Lokale Artikelnummer::
APOSOR89540-50MG
Beschreibung:
4-(4-(8-Oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(1,4-dioxaspiro[4.5]decan-8-yl)-1H-pyrazolo[3,4-d]pyrimidin-6-yl)aniline 50mg pack 1 * 50 mg
VE:
1 * 50 mg
New Product
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4'-Amino-2'-hydroxyacetophenon
Lieferant:
Alfa Aesar
Beschreibung:
5-Chlor-1-(4-piperidinyl)-2-benzimidazolidinon ≥98%
Artikel-Nr:
(BOSSBS-6110R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6110R-HRP
Lokale Artikelnummer::
BOSSBS-6110R-HRP
Beschreibung:
SPARC (secreted protein acidic and rich in cysteine) is a phosphorylated, acidic, glycine-rich glycoprotein that is secreted by endothelial cells and is present in large amounts in the parietal endoderm of mouse embryos and in human placenta. SPARC-like protein 1 (SPARCL1), also known as high endothelial venule protein (Hevin) or MAST9, is a 664 amino acid member of the SPARC family of proteins. Highly expressed in lymph node, heart, lung, brain, skeletal muscle, ovary, colon and small intestine, SPARCL1 is a secreted protein that contains one EF-hand domain, one follistatin-like domain and one Kazal-like domain. SPARCL1 is implicated to play a role in neuronal remodeling and tumor suppression. The gene encoding SPARCL1 maps to chromosome 4q22.1.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6110R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6110R-A350
Lokale Artikelnummer::
BOSSBS-6110R-A350
Beschreibung:
SPARC (secreted protein acidic and rich in cysteine) is a phosphorylated, acidic, glycine-rich glycoprotein that is secreted by endothelial cells and is present in large amounts in the parietal endoderm of mouse embryos and in human placenta. SPARC-like protein 1 (SPARCL1), also known as high endothelial venule protein (Hevin) or MAST9, is a 664 amino acid member of the SPARC family of proteins. Highly expressed in lymph node, heart, lung, brain, skeletal muscle, ovary, colon and small intestine, SPARCL1 is a secreted protein that contains one EF-hand domain, one follistatin-like domain and one Kazal-like domain. SPARCL1 is implicated to play a role in neuronal remodeling and tumor suppression. The gene encoding SPARCL1 maps to chromosome 4q22.1.
VE:
1 * 100 µl
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:
(R)-(+)-4-Benzyl-2-oxazolidinon
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
Artikel-Nr:
(BOSSBS-9380R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9380R-HRP
Lokale Artikelnummer::
BOSSBS-9380R-HRP
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
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3',5'-Dimethoxy-4'-hydroxyacetophenon 99%
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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