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3-Bromo-4-chloro-5-(trifluoromethyl)phenylacetic+acid
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3-Bromo-4-chloro-5-(trifluoromethyl)phenylacetic+acid
Artikel-Nr:
(BWRLBS3546)
Lieferant:
Bioworld Technology
Hersteller-Artikelnummer::
BS3546
Lokale Artikelnummer::
BWRLBS3546
Beschreibung:
Synthetic peptide, corresponding to amino acids 11-60 of Human Insulin.
VE:
1 * 100 µG
Artikel-Nr:
(BWRLBS5529)
Lieferant:
Bioworld Technology
Hersteller-Artikelnummer::
BS5529
Lokale Artikelnummer::
BWRLBS5529
Beschreibung:
Synthetic peptide, corresponding to amino acids 11-60 of Human p53.
VE:
1 * 100 µG
Artikel-Nr:
(BOSSBS-11518R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11518R-CY5
Lokale Artikelnummer::
BOSSBS-11518R-CY5
Beschreibung:
Preferentially catalyzes the conversion of 11-deoxycorticosterone to aldosterone via corticosterone and 18-hydroxycorticosterone.
VE:
1 * 100 µl
Lieferant:
VWR Chemicals
Beschreibung:
Diese Standards können für die Kalibrierung, Kontrolle, Verifizierung, Qualifikation oder methodische Validierung von kinematischen oder dynamischen Viskositätsmessgeräten (manuell und automatisch) verwendet werden. Jeder Standard ist für kinematische Viskosität (mm²/s, cSt), dynamische Viskosität (cP) und Dichte (g/ml) bei verschiedenen Temperaturen zertifiziert.
Lieferant:
Alfa Aesar
Beschreibung:
5-Brom-2-fluorpyridin ≥98%
Artikel-Nr:
(BOSSBS-9659R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9659R-CY3
Lokale Artikelnummer::
BOSSBS-9659R-CY3
Beschreibung:
With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and β thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11. The FAM76B gene product has been provisionally designated FAM76B pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(1294987.)
Lieferant:
USP
Hersteller-Artikelnummer::
1294987
Lokale Artikelnummer::
USPH1294987
Beschreibung:
USP Reference Standards are specified for use in conducting official USP–NF tests and assays. USP also provides Reference Standards specified in the Food Chemicals Codex as well as authentic substances—high-quality chemical samples—as a service to analytical, clinical, pharmaceutical and research laboratories. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.
VE:
1 * 100 mg
Artikel-Nr:
(1161509.)
Lieferant:
USP
Hersteller-Artikelnummer::
1161509
Lokale Artikelnummer::
USPH1161509
Beschreibung:
USP Reference Standards are specified for use in conducting official USP–NF tests and assays. USP also provides Reference Standards specified in the Food Chemicals Codex as well as authentic substances—high-quality chemical samples—as a service to analytical, clinical, pharmaceutical and research laboratories. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.
VE:
1 * 600 mg
Artikel-Nr:
(APOSOR70075-100G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR70075-100G
Lokale Artikelnummer::
APOSOR70075-100G
Beschreibung:
1,1,3,3-Tetramethyldisilazan
VE:
1 * 100 g
Artikel-Nr:
(APOSOR3057-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR3057-1G
Lokale Artikelnummer::
APOSOR3057-1G
Beschreibung:
4-Brom-o-toluonitril
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-8225R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8225R-HRP
Lokale Artikelnummer::
BOSSBS-8225R-HRP
Beschreibung:
FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8225R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8225R-A647
Lokale Artikelnummer::
BOSSBS-8225R-A647
Beschreibung:
FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:
1 * 100 µl
Lieferant:
Tonbo Biosciences
Beschreibung:
The UC10-4F10-11 antibody is specific for mouse CD152, commonly known as CTLA-4, a 33-37 kDa protein expressed as a homodimer on the surface of activated T and B cells, and on thymocytes. CTLA-4 is structurally similar, yet functionally disparate, to the T cell co-stimulatory molecule CD28. Both CTLA-4 and CD28 interact with the co-stimulatory molecules CD80 (B7-1) and CD86 (B7-2) on antigen-presenting cells, with CTLA-4 displaying a higher avidity than CD28. While CD28 typically delivers a potent co-stimulatory signal in support of T cell activation, CTLA-4 appears to act as a negative regulator of T cell activation and may contribute to the suppressor function of Treg cells.
Lieferant:
BLD PHARMATECH GMBH
Beschreibung:
3,3',5,5'-Tetramethyl-2,2'-biphenol 97%
Lieferant:
Thermo Scientific
Beschreibung:
2,2'-Bis(trifluoromethyl)benzidine 97%
Artikel-Nr:
(BOSSBS-9937R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9937R-A680
Lokale Artikelnummer::
BOSSBS-9937R-A680
Beschreibung:
C11orf24, also known as DM4E3, is a 449 amino acid single-pass type I membrane protein that is expressed in brain, lung, skeletal muscle, kidney, spleen, prostate, testis, ovary and small intestine, with highest expression in heart, placenta, liver, pancreas and colon, and low expression in thymus and leukocytes. C11orf24 is encoded by a gene located on human chromosome 11, which consists of approximately 135 million base pairs and 1400 genes. Chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumours, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
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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