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4-(4-Methylpiperazin-1-yl)benzoic+acid
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4-(4-Methylpiperazin-1-yl)benzoic+acid
Artikel-Nr:
(BOSSBS-9614R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9614R-FITC
Lokale Artikelnummer::
BOSSBS-9614R-FITC
Beschreibung:
Chromosome 14 contains about 700 genes and 106 million base pairs and makes up about 3.5% of human cellular DNA. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease. The SERPINA1 gene is located on chromosome 14 and when defective leads to the genetic disorder ?-antitrypsin deficiency. This disorder is characterized by severe lung complications and liver dysfunction. Notably, the immunoglobulin heavy chain locus is found on chromosome 14 and has been identified as a fusion with the chromosome 19 encoded protein BCL3 in the (14;19) translocations found in a variety of B cell malignancies. The C14orf140 gene product has been provisionally designated C14orf140 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8262R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8262R-CY5.5
Lokale Artikelnummer::
BOSSBS-8262R-CY5.5
Beschreibung:
DHRS7 (dehydrogenase/reductase (SDR family) member 7), also known as SDR34C1, CGI-86 or retSDR4, is a 339 amino acid member of the SDR family. Like other members of the SDR family, DHRS7 contains a cofactor-binding Rossman-fold domain and is thought to catalyze the oxidation and reduction of a variety of substrates such as steroids and retinoids. DHRS7 exists as two alternatively spliced isoforms that are encoded by a gene located on human chromosome 14, which houses over 700 genes and comprises nearly 3.5% of the human genome. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease (AD). The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder ?-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6831R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6831R
Lokale Artikelnummer::
BOSSBS-6831R
Beschreibung:
Programmed cell death regulates a number of biological processes such as normal organism development, tissue homeostasis, and removal of damaged cells. Disruption of this process has been implicated in a variety of diseases such as cancer. FAIM2 is a recently identified protein that can inhibit the apoptotic signal transduced by the Fas receptor but not from the related tumor necrosis factor-alpha death signal. In this respect, FAIM2 is functionally similar to the anti-apoptotic proteins FAIM, FLIP and Bcl-xL. FAIM2, a seven membrane spanning protein, can bind the Fas receptor but does not regulate Fas expression or inhibit binding of FADD to Fas. FAIM2 is widely distributed, but highly expressed in the hippocampus and other neural tissues. FAIM2 was also identified as the neural membrane protein 35 (NMP35) and its expression is known to be regulated by the Phosphatidylinositol 3-kinase-Akt/PKB pathway.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8262R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8262R-CY7
Lokale Artikelnummer::
BOSSBS-8262R-CY7
Beschreibung:
DHRS7 (dehydrogenase/reductase (SDR family) member 7), also known as SDR34C1, CGI-86 or retSDR4, is a 339 amino acid member of the SDR family. Like other members of the SDR family, DHRS7 contains a cofactor-binding Rossman-fold domain and is thought to catalyze the oxidation and reduction of a variety of substrates such as steroids and retinoids. DHRS7 exists as two alternatively spliced isoforms that are encoded by a gene located on human chromosome 14, which houses over 700 genes and comprises nearly 3.5% of the human genome. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease (AD). The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder ?-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11733R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11733R-CY5
Lokale Artikelnummer::
BOSSBS-11733R-CY5
Beschreibung:
Myotubularin and the myotubularin-related proteins (MTMR1-9) belong to a highly conserved family of eukaryotic phosphatases. They are protein tyrosine phosphatases that utilize inositol phospholipids, rather than phosphoproteins, as substrates. MTMR family members hydrolyze both Phosphatidylinositol 3-phosphate (PtdIns3P) and PtdIns(3,5)P2. MTMR2 interacts with MTMR5, an inactive family member that increases the enzymatic activity of MTMR2 and dictates its subcellular localization. Mutations in MTMR2 cause autosomal recessive Charcot-Marie-Tooth type 4B1 (CMT4B1), which is characterized by reduced nerve conduction velocities, focally folded myelin sheaths and demyelination. MTMR3 and MTMR4 can either interact with each other or self associate. MTMR6 regulates the activity of the calcium-activated potassium channel 3.1. MTMR9 regulates the activity of MTMR7 and MTMR8.
VE:
1 * 100 µl
Artikel-Nr:
(ABCRAB120715.0025)
Lieferant:
ABCR
Hersteller-Artikelnummer::
AB120715.0025
Lokale Artikelnummer::
ABCRAB120715.0025
Beschreibung:
Metal Beta-diketonates, Metal TMHD, Volatile Precursors for CVD
VE:
1 * 25 "
 This is a MarketSource item. Additional charges may apply
Lieferant:
Alfa Aesar
Beschreibung:
4-[(2,4-Dimethoxyphenyl)-(fmoc-amino)methyl]phenoxyacetic acid ≥98%
Artikel-Nr:
(BOSSBS-6514R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6514R
Lokale Artikelnummer::
BOSSBS-6514R
Beschreibung:
CGI-99 is a 244 amino acid protein that localizes to the nucleus, as well as to the cytoplasm, and belongs to the UPF0568 family. Expressed in a variety of tissues with particularly high levels in heart and skeletal muscle, CGI-99 functions as a homodimer that interacts with Ninein and is thought to regulate Ninein function. CGI-99 is overexpressed in brain tumor tissue, suggesting a role in tumor development and metastasis. The gene encoding CGI-99 maps to human chromosome 14, which houses over 700 genes and comprises nearly 3.5% of the human genome. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease (AD). The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder ?-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
4-[(tert-Butoxycarbonylamino)methyl]phenylboronic acid pinacol ester 97%
Lieferant:
MP Biomedicals
Beschreibung:
Colorimetric reagent for iron, manganese, titanium, and molybdenum. Complexing agent.
Artikel-Nr:
(ABCRAB123782.0001)
Lieferant:
ABCR
Hersteller-Artikelnummer::
AB123782.0001
Lokale Artikelnummer::
ABCRAB123782.0001
Beschreibung:
Metal Beta-diketonates, Metal TMHD, Volatile Precursors for CVD
VE:
1 * 1 g
This is a MarketSource item. Additional charges may apply
Lieferant:
Alfa Aesar
Beschreibung:
Excellent colorimetric substrate for detection of horseradish peroxidase labelled probes; particularly useful in ELISA techniques, blue result can be read spectrophotometrically at 370 or 650 nm3,3',5,5'-Tetramethylbenzidine is used as a clinical reagent for testing blood.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Dichlorobis[di-tert-butyl(4-dimethylaminophenyl)phosphine]palladium(II) 97%
Lieferant:
Bernd Kraft
Beschreibung:
Kaliumchlorid 3.5 mol/l (3.5 N) in wässriger Lösung
Lieferant:
COMBI-BLOCKS
Beschreibung:
2-Chlor-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyridin
Lieferant:
COMBI-BLOCKS
Beschreibung:
3-Chlor-2-(3,5-dimethyl-1H-pyrazol-1-yl)pyridin
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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