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2-Methyl-4-isothiazolin-3-one+hydrochloride
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125 289 results were found
2-Methyl-4-isothiazolin-3-one+hydrochloride
Lieferant:
Thermo Scientific
Beschreibung:
4'-Nitroacetophenon 97%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-(Trifluoromethyl)-1-indanone
Lieferant:
Thermo Scientific
Beschreibung:
4-Acryloylmorpholine 97%
Artikel-Nr:
(BLDPBD2012-10G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD2012-10G
Lokale Artikelnummer::
BLDPBD2012-10G
Beschreibung:
7-(4-Brombutoxy)-3,4-dihydro-2(1H)-chinolinon 97%
VE:
1 * 10 g
Artikel-Nr:
(APOSBIDF1016-5MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
BIDF1016-5MG
Lokale Artikelnummer::
APOSBIDF1016-5MG
Beschreibung:
Marein with hplc
VE:
1 * 5 mg
Lieferant:
Thermo Scientific
Beschreibung:
2',4'-Dichloracetophenon 97%
Artikel-Nr:
(BOSSBS-9616R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9616R
Lokale Artikelnummer::
BOSSBS-9616R
Beschreibung:
Ubr7 is a 425 amino acid protein that contains one UBR-type zinc finger and one PHD zinc finger. Participating in protein modification events within the N-end rule pathway, Ubr7 functions as an E3 ubiquitin-protein ligase that recognizes and binds proteins that contain destabilizing N-terminal residues, thereby leading to their ubiquitination and subsequent degradation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4820R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4820R-HRP
Lokale Artikelnummer::
BOSSBS-4820R-HRP
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. Dephosphorylates LYN, and thereby modulates LYN activity (By similarity).
VE:
1 * 100 µl
Artikel-Nr:
(APOSPC6302-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC6302-1G
Lokale Artikelnummer::
APOSPC6302-1G
Beschreibung:
2-(Trifluoromethyl)xanthone
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-4820R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4820R-CY5
Lokale Artikelnummer::
BOSSBS-4820R-CY5
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. Dephosphorylates LYN, and thereby modulates LYN activity (By similarity).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4820R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4820R-A488
Lokale Artikelnummer::
BOSSBS-4820R-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. Dephosphorylates LYN, and thereby modulates LYN activity (By similarity).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9161R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9161R-FITC
Lokale Artikelnummer::
BOSSBS-9161R-FITC
Beschreibung:
The tripartite motif (TRIM) family of proteins are characterized by a conserved TRIM domain that includes a coiled-coil region, a B-box type zinc finger, one RING finger and three zinc-binding domains. TRIM17 (tripartite motif-containing 17), also known as RBCC, terf or RNF16, is a 477 amino acid protein that contains one RING-type zinc finger, one SPRY domain and one B box-type zinc finger. Expressed nearly exclusively in testis, TRIM17 belongs to the TRIM family and, based on its functional domains, may play a role in transcriptional regulation events. The gene encoding TRIM17 maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.
VE:
1 * 100 µl
Artikel-Nr:
(MOLE61642496-500G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
61642496-500G
Lokale Artikelnummer::
MOLE61642496-500G
Beschreibung:
(3-Chlorpropyl)dimethylammoniumchlorid
VE:
1 * 500 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BOSSBS-11622R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11622R
Lokale Artikelnummer::
BOSSBS-11622R
Beschreibung:
Polycystin-1L3 is a 1,732 amino acid multi-pass membrane protein that contains one PLAT domain, one GPS domain and one C-type lectin domain. Expressed at high levels in placenta and present at lower levels in lung and heart, Polycystin-1L3 is thought to function as an ion-channel regulator that may interact with Polycystin-L and play a role in heteromeric taste channels. The gene encoding Polycystin-1L3 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11622R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11622R-CY5
Lokale Artikelnummer::
BOSSBS-11622R-CY5
Beschreibung:
Polycystin-1L3 is a 1,732 amino acid multi-pass membrane protein that contains one PLAT domain, one GPS domain and one C-type lectin domain. Expressed at high levels in placenta and present at lower levels in lung and heart, Polycystin-1L3 is thought to function as an ion-channel regulator that may interact with Polycystin-L and play a role in heteromeric taste channels. The gene encoding Polycystin-1L3 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
VE:
1 * 100 µl
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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