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Tetrabutylazanium+trifluoro(3-fluorophenyl)boranuide
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Tetrabutylazanium+trifluoro(3-fluorophenyl)boranuide
Artikel-Nr:
(HONE04248.9025)
Lieferant:
Honeywell Chemicals
Hersteller-Artikelnummer::
04248.9025
Lokale Artikelnummer::
HONE04248.9025
Beschreibung:
di-Kaliumhydrogenphosphat
VE:
1 * 25 kg
Artikel-Nr:
(HONE25413.9050)
Lieferant:
Honeywell Chemicals
Hersteller-Artikelnummer::
25413.9050
Lokale Artikelnummer::
HONE25413.9050
Beschreibung:
di-Kaliumoxalat Monohydrat ≥99%, puriss., reinst
VE:
1 * 50 kg
Lieferant:
Sigma-Aldrich
Beschreibung:
Galliumnitrid, Sigma-Aldrich®
Artikel-Nr:
(ABCRAB255209.0500)
Lieferant:
ABCR
Hersteller-Artikelnummer::
AB255209.0500
Lokale Artikelnummer::
ABCRAB255209.0500
Beschreibung:
Digadoliniumtrioxid
VE:
1 * 500 g
 This is a MarketSource item. Additional charges may apply
Lieferant:
Honeywell Chemicals
Beschreibung:
Concentrate for 1L standard solution
Artikel-Nr:
(PRSI25-261)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
25-261
Lokale Artikelnummer::
PRSI25-261
Beschreibung:
KCNJ1 has a greater tendency to allow potassium to flow into a cell rather than out of a cell. Mutations in this gene have been associated with antenatal Bartter syndrome, which is characterized by salt wasting, hypokalemic alkalosis, hypercalciuria, and low blood pressure. Multiple transcript variants encoding different isoforms have been found for KCNJ1.Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. It is activated by internal ATP and probably plays an important role in potassium homeostasis.Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. It is activated by internal ATP and probably plays an important role in potassium homeostasis. The encoded protein has a greater tendency to allow potassium to flow into a cell rather than out of a cell. Mutations in this gene have been associated with antenatal Bartter syndrome, which is characterized by salt wasting, hypokalemic alkalosis, hypercalciuria, and low blood pressure. Multiple transcript variants encoding different isoforms have been found for this gene.
VE:
1 * 50 µG
Artikel-Nr:
(SPCMP1309-25GM)
Lieferant:
Spectrum Chemical
Hersteller-Artikelnummer::
P1309-25GM
Lokale Artikelnummer::
SPCMP1309-25GM
Beschreibung:
Potassium Iodate, FCC is used as a source for dietary iodine. The FCC grade meets the requirements of the Food Chemical Codex indicates and is suitable for all food, beverage and nutritional supplement applications. Spectrum Chemical offers over 300 Food grade chemical ingredients packaged in laboratory size bottles to production drum quantities and are manufactured, packaged and stored under current Good Manufacturing Practices (cGMP) per 21CFR part 211 in FDA registered and inspected facilities.
VE:
1 * 25 g
Artikel-Nr:
(HACH1430598)
Lieferant:
Hach
Hersteller-Artikelnummer::
1430598
Lokale Artikelnummer::
HACH1430598
Beschreibung:
Buffered dilution water required for testing recreational, drinking and wastewater.
VE:
1 * 25 ST
Artikel-Nr:
(CHMP003018.0025)
Lieferant:
CHEMPUR
Hersteller-Artikelnummer::
003018.0025
Lokale Artikelnummer::
CHMP003018.0025
Beschreibung:
Erbiumtrinitrat Pentahydrat
VE:
1 * 25 g
Artikel-Nr:
(SIAL289272-25G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
289272-25G
Lokale Artikelnummer::
SIAL289272-25G
Beschreibung:
Dysprosiumtrichlorid Hexahydrat, Sigma-Aldrich®
VE:
1 * 25 g
Artikel-Nr:
(USBI124634)
Lieferant:
US Biological
Hersteller-Artikelnummer::
124634
Lokale Artikelnummer::
USBI124634
Beschreibung:
Anti-CD44 Mouse Monoclonal Antibody [clone: 1E1]
VE:
1 * 100 µG
Lieferant:
Merck
Beschreibung:
tri-Kaliumcitrat Monohydrat 99,0-100,5% (durch Perchlorsäure-Titration), EMPROVE® ESSENTIAL Ph. Eur., BP, USP, FCC, E332, SAFC®
Artikel-Nr:
(BOSSBS-7116R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7116R-A350
Lokale Artikelnummer::
BOSSBS-7116R-A350
Beschreibung:
Ro autoantigens are of clinical significance because directed against them are found in most patients with primary Sjqgren syndrome, subacute cutaneous lupus erythematosus (SLE), neonatal lupus erythematosus, ANA-negative lupus erythematosus, and systemic lupus erythematosus-like disease secondary to homozygous C2 or C4 complement deficiency (1). Ro/SSA is a ribonucleoprotein that binds to auto in 35 to 50% of patients with SLE and in up to 97% of patients with Sjqgren syndrome (2). The Ro/SSA particle consists of a single immunoreactive protein noncovalently bound with one of four small RNA molecules (2). Most anti-Ro/SSA-positive sera detect not only the main protein, but also a smaller Ro/SSA protein (2). The genes which encode the smaller and larger proteins map to human chromosomes 11p15.5 and 1q31, respectively (3?). La/SSB is an autoimmune RNA-binding protein that plays a role in the transcription of RNA polymerase III was originally defined by its reactivity with auto from patients with Sjé°ƒren syndrome and SLE (6).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9380R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9380R-A555
Lokale Artikelnummer::
BOSSBS-9380R-A555
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-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9380R-A680
Lokale Artikelnummer::
BOSSBS-9380R-A680
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 characterised 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:
Sigma-Aldrich
Beschreibung:
Erbiumtrinitrat Pentahydrat, Sigma-Aldrich®
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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