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Ethyl+3-(4-Isobutylphenyl)acrylate
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Ethyl+3-(4-Isobutylphenyl)acrylate
Artikel-Nr:
(BOSSBS-9741R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9741R-A680
Lokale Artikelnummer::
BOSSBS-9741R-A680
Beschreibung:
ANGEL1, also known as KIAA0759, is a 670 amino acid protein belonging to the CKR-4 protein family. ANGEL1 is encoded by a gene located on human chromosome 14, which contains about 700 genes and 106 million base pairs, making up about 3.5% of human cellular DNA. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of 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 characterised by severe lung complications and liver dysfunction. Notably, the immunoglobulin heavy chain locus on chromosome 14 and its fusion via translocation with the chromosome 19 encoded protein BCL3 may be related to B-cell malignancies.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9741R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9741R-A750
Lokale Artikelnummer::
BOSSBS-9741R-A750
Beschreibung:
ANGEL1, also known as KIAA0759, is a 670 amino acid protein belonging to the CKR-4 protein family. ANGEL1 is encoded by a gene located on human chromosome 14, which contains about 700 genes and 106 million base pairs, making up about 3.5% of human cellular DNA. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of 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 characterised by severe lung complications and liver dysfunction. Notably, the immunoglobulin heavy chain locus on chromosome 14 and its fusion via translocation with the chromosome 19 encoded protein BCL3 may be related to B-cell malignancies.
VE:
1 * 100 µl
Lieferant:
COMBI-BLOCKS
Beschreibung:
2-Benzyloxy-3,5-difluorphenylboronsäure
Artikel-Nr:
(FLUO018571-5G)
Lieferant:
FLUOROCHEM
Hersteller-Artikelnummer::
018571-5G
Lokale Artikelnummer::
FLUO018571-5G
Beschreibung:
3,5-Dimethoxybenzhydrazid
VE:
1 * 5 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(SIAL386367-25G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
386367-25G
Lokale Artikelnummer::
SIAL386367-25G
Beschreibung:
Methyl-3,5-dinitrobenzoat, Sigma-Aldrich®
VE:
1 * 25 g
Lieferant:
FLUOROCHEM
Beschreibung:
2-(3,5-Dimethyl-1H-pyrazol-4-yl)benzoesäure
Lieferant:
Sigma-Aldrich
Beschreibung:
(3,5-Dimethoxy-4-hydroxyphenyl)essigsäure, Sigma-Aldrich®
Lieferant:
Biotium
Beschreibung:
This antibody recognizes a protein of 35 kDa, which is identified as tartrate-resistant acid phosphatase (TRAcP). It exists as two isoforms (5a and 5b). This MAb reacts with both the isoforms. Serum TRAcP 5a is secreted by macrophages and dendritic cells and increased in many patients of rheumatoid arthritis.Serum TRAcP 5b is produced from osteoclasts and elevated during bone resorption. TRAcP is an iron containing glycoprotein, which catalyzes the conversion of orthophosphoric monoester to alcohol and orthophosphate. It is the most basic of the acid phosphatases and is the only form not inhibited by L( )-tartrate. TRAcP is synthesized as a latent proenzyme and is activated by proteolytic cleavage and reduction. Normally, TRAcP is highly expressed by osteoclasts, activated macrophages, neurons and endometrium during pregnancy. Expression of TRAcP is increased in certain pathological conditions such as Leukemic Reticuloendotheliosis (Hairy Cell Leukemia), Gaucher's Disease, HIV-induced Encephalopathy, Osteoclastoma and in osteoporosis and metabolic bone diseases. Anti-TRAcP antibody labels the cells of Hairy Cell Leukemia (HCL) with a high degree of sensitivity and specificity. Other cells stained with this antibody are tissue macrophages and osteoclasts.
Artikel-Nr:
(MOLE82959542-100G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
82959542-100G
Lokale Artikelnummer::
MOLE82959542-100G
Beschreibung:
Methyl-3,5-dimethoxybenzoat
VE:
1 * 100 g
This is a MarketSource item. Additional charges may apply
Lieferant:
Sigma-Aldrich
Beschreibung:
3,5-Bis(trifluormethyl)benzoesäure, Sigma-Aldrich®
Artikel-Nr:
(SIAL273023-5G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
273023-5G
Lokale Artikelnummer::
SIAL273023-5G
Beschreibung:
3,5-Di-tert-butylbenzoesäure, Sigma-Aldrich®
VE:
1 * 5 g
Lieferant:
Thermo Scientific
Beschreibung:
Methyl-3,5-dihydroxybenzoat
Artikel-Nr:
(BOSSBS-8260R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8260R-A647
Lokale Artikelnummer::
BOSSBS-8260R-A647
Beschreibung:
DHRS1 (dehydrogenase/reductase (SDR family) member 1), also known as SDR19C1, is a 313 amino acid protein that belongs to the short-chain dehydrogenases/reductases (SDR) family and likely functions as an oxidoreductase. Abundantly expressed in heart and liver, DHRS1 contains an SDR motif and is encoded by a gene that maps to human chromosome 14q12. Human chromosome 14 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-8260R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8260R-A350
Lokale Artikelnummer::
BOSSBS-8260R-A350
Beschreibung:
DHRS1 (dehydrogenase/reductase (SDR family) member 1), also known as SDR19C1, is a 313 amino acid protein that belongs to the short-chain dehydrogenases/reductases (SDR) family and likely functions as an oxidoreductase. Abundantly expressed in heart and liver, DHRS1 contains an SDR motif and is encoded by a gene that maps to human chromosome 14q12. Human chromosome 14 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-8409R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8409R-A488
Lokale Artikelnummer::
BOSSBS-8409R-A488
Beschreibung:
GLB1L3 is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family. GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25. 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. 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-8409R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8409R-A680
Lokale Artikelnummer::
BOSSBS-8409R-A680
Beschreibung:
GLB1L3 is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family. GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25. 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. 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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