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2-(1H-Imidazol-1-yl)isonicotinic+acid
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2-(1H-Imidazol-1-yl)isonicotinic+acid
Artikel-Nr:
(BOSSBS-9380R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9380R-FITC
Lokale Artikelnummer::
BOSSBS-9380R-FITC
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:
(MOLE13713550-500G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
13713550-500G
Lokale Artikelnummer::
MOLE13713550-500G
Beschreibung:
2-Chlorethylammoniumchlorid
VE:
1 * 500 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BOSSBS-11622R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11622R-CY3
Lokale Artikelnummer::
BOSSBS-11622R-CY3
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:
(141-1431)
Lieferant:
CONTEC
Hersteller-Artikelnummer::
2940P3S
Lokale Artikelnummer::
CONT2940P3S
Beschreibung:
The autoclavable "Compact Bucket System" is an all-in-one solution to make cleaning and disinfecting easier and more efficient. The trolley is designed for use with Contec's VertiKlean® MAX™, VertiKlean® MAX™ Sealed Edge, and QuickTask™ Mopping Systems.
VE:
1 * 1 ST
Lieferant:
Thermo Scientific
Beschreibung:
2-Ethylphenylhydraziniumchlorid
Lieferant:
Sigma-Aldrich
Beschreibung:
3-Nitrophenylhydraziniumchlorid, Sigma-Aldrich®
Artikel-Nr:
(HONCR1505-10MG)
Lieferant:
Honeywell Chemicals
Hersteller-Artikelnummer::
R1505-10MG
Lokale Artikelnummer::
HONCR1505-10MG
Beschreibung:
High quality inorganic and organic reference materials produced according to ISO 9001.
VE:
1 * 10 mg
Lieferant:
Sigma-Aldrich
Beschreibung:
p-Toluidiniumchlorid, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-9161R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9161R-CY5
Lokale Artikelnummer::
BOSSBS-9161R-CY5
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
Lieferant:
MACRON AVANTOR BRAND
Beschreibung:
Aceton ≥99,0% Ph. Eur., Macron Fine Chemicals™
Artikel-Nr:
(BOSSBS-9256R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9256R-CY3
Lokale Artikelnummer::
BOSSBS-9256R-CY3
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. RNF113B (ring finger protein 113B), also referred to as zinc finger protein 183-like 1, RNF161, MGC26599, bA10G5.1 or ZNF183L1, is a 322 amino acid protein containing one C3H1-type zinc finger and one RING-type zinc finger. The gene encoding RNF113B maps to human chromosome 13, which houses over 400 genes, such as BRCA2 and RB1, and comprises nearly 4% of the human genome. Trisomy 13, also known as Patau syndrome, is deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9256R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9256R-CY5.5
Lokale Artikelnummer::
BOSSBS-9256R-CY5.5
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. RNF113B (ring finger protein 113B), also referred to as zinc finger protein 183-like 1, RNF161, MGC26599, bA10G5.1 or ZNF183L1, is a 322 amino acid protein containing one C3H1-type zinc finger and one RING-type zinc finger. The gene encoding RNF113B maps to human chromosome 13, which houses over 400 genes, such as BRCA2 and RB1, and comprises nearly 4% of the human genome. Trisomy 13, also known as Patau syndrome, is deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections.
VE:
1 * 100 µl
Lieferant:
Merck
Beschreibung:
L-Lysine Monohydrochlorid, EMPROVE® EXPERT Ph. Eur., BP, USP geeignet für die Verwendung als Trägerstoff, SAFC®
Artikel-Nr:
(BOSSBS-9161R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9161R-HRP
Lokale Artikelnummer::
BOSSBS-9161R-HRP
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:
(BOSSBS-9161R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9161R-A750
Lokale Artikelnummer::
BOSSBS-9161R-A750
Beschreibung:
The tripartite motif (TRIM) family of proteins are characterised 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
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
PDA is a superior crosslinker for Page Gels, gives a reduction of silver stain background while increasing thephysical strength and giving improved electrophoratic separations.
Preis auf Anfrage
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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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