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3,5-Dioxocyclohexanecarboxylic+acid
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3,5-Dioxocyclohexanecarboxylic+acid
Artikel-Nr:
(SIAL499501-5G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
499501-5G
Lokale Artikelnummer::
SIAL499501-5G
Beschreibung:
3,5-Dibromphenylboronsäure, Sigma-Aldrich®
VE:
1 * 5 g
Lieferant:
COMBI-BLOCKS
Beschreibung:
3,5-Dichlorphenylboronsäure
Artikel-Nr:
(BOSSBS-13234R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13234R-CY5
Lokale Artikelnummer::
BOSSBS-13234R-CY5
Beschreibung:
The mammalian FXYD family maintains Na+ and K+ gradients between the intracellular and extracellular milieus of cells in processes such as renal Na+-reabsorption, muscle contraction and neuronal excitability. FXYDs are single-span membrane proteins that share a 35 amino acid signature domain, beginning with the sequence PFXYD and containing seven invariant and six conserved amino acids. Members of the FXYD family include FXYD1 (PLM, phospholemman), FXYD2 (the g subunit of the Na+/K+-ATPase), FXYD3 (Mat8, mammary tumor protein), FXYD4 (CHIF) and FXYD5 (RIC). FXYD6 is expressed in various epithelial cells bordering the endolymph space and in the auditory neurons. FXYD6 co-localizes with Na+/K+-ATPase in the stria vascularis and can be co-immunoprecipitated with Na+/K+-ATPase. After expression, FXYD6 associates with Na+/K+-ATPase alpha1-beta1 and alpha1-beta2 isozymes, which are preferentially expressed in different regions of the inner ear and also with gastric and non-gastric H+/K+-ATPase.
VE:
1 * 100 µl
Artikel-Nr:
(SIAL128848-500G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
128848-500G
Lokale Artikelnummer::
SIAL128848-500G
Beschreibung:
3,5-Dinitrosalicylsäure, Sigma-Aldrich®
VE:
1 * 500 g
Lieferant:
COMBI-BLOCKS
Beschreibung:
3,5-Dinitrophenylboronsäurepinakolester
Artikel-Nr:
(BOSSBS-8226R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8226R-CY5
Lokale Artikelnummer::
BOSSBS-8226R-CY5
Beschreibung:
FAM161B is a 647 amino acid protein that belongs to the FAM161 family. The gene that encodes FAM161B consists of approximately 16,413 bases and maps to human chromosome 14q24.3. Housing over 700 genes, chromosome 14 comprises nearly 3.5% of the human genome. Chromosome 14 encodes the Presenilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer’s disease. The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder α1-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction. An inversion of the long arm of chromosome 14 is thought to be involved in T-cell chronic lymphocytic leukemia (CLL), a cancer that affects T lymphocytes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13235R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13235R
Lokale Artikelnummer::
BOSSBS-13235R
Beschreibung:
This reference sequence was derived from multiple replicate ESTs and validated by similar human genomic sequence. This gene encodes a member of a family of small membrane proteins that share a 35-amino acid signature sequence domain, beginning with the sequence PFXYD and containing 7 invariant and 6 highly conserved amino acids. The approved human gene nomenclature for the family is FXYD-domain containing ion transport regulator. Transmembrane topology has been established for two family members (FXYD1 and FXYD2), with the N-terminus extracellular and the C-terminus on the cytoplasmic side of the membrane. FXYD2, also known as the gamma subunit of the Na,K-ATPase, regulates the properties of that enzyme. FXYD1 (phospholemman), FXYD2 (gamma), FXYD3 (MAT-8), FXYD4 (CHIF), and FXYD5 (RIC) have been shown to induce channel activity in experimental expression systems. This gene product, FXYD7, is novel and has not been characterized as a protein. [RefSeq curation by Kathleen J. Sweadner, Ph.D., sweadner@helix.mgh.harvard.edu., Dec 2000].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13234R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13234R-CY3
Lokale Artikelnummer::
BOSSBS-13234R-CY3
Beschreibung:
The mammalian FXYD family maintains Na+ and K+ gradients between the intracellular and extracellular milieus of cells in processes such as renal Na+-reabsorption, muscle contraction and neuronal excitability. FXYDs are single-span membrane proteins that share a 35 amino acid signature domain, beginning with the sequence PFXYD and containing seven invariant and six conserved amino acids. Members of the FXYD family include FXYD1 (PLM, phospholemman), FXYD2 (the g subunit of the Na+/K+-ATPase), FXYD3 (Mat8, mammary tumor protein), FXYD4 (CHIF) and FXYD5 (RIC). FXYD6 is expressed in various epithelial cells bordering the endolymph space and in the auditory neurons. FXYD6 co-localizes with Na+/K+-ATPase in the stria vascularis and can be co-immunoprecipitated with Na+/K+-ATPase. After expression, FXYD6 associates with Na+/K+-ATPase alpha1-beta1 and alpha1-beta2 isozymes, which are preferentially expressed in different regions of the inner ear and also with gastric and non-gastric H+/K+-ATPase.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13234R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13234R-CY7
Lokale Artikelnummer::
BOSSBS-13234R-CY7
Beschreibung:
The mammalian FXYD family maintains Na+ and K+ gradients between the intracellular and extracellular milieus of cells in processes such as renal Na+-reabsorption, muscle contraction and neuronal excitability. FXYDs are single-span membrane proteins that share a 35 amino acid signature domain, beginning with the sequence PFXYD and containing seven invariant and six conserved amino acids. Members of the FXYD family include FXYD1 (PLM, phospholemman), FXYD2 (the g subunit of the Na+/K+-ATPase), FXYD3 (Mat8, mammary tumor protein), FXYD4 (CHIF) and FXYD5 (RIC). FXYD6 is expressed in various epithelial cells bordering the endolymph space and in the auditory neurons. FXYD6 co-localizes with Na+/K+-ATPase in the stria vascularis and can be co-immunoprecipitated with Na+/K+-ATPase. After expression, FXYD6 associates with Na+/K+-ATPase alpha1-beta1 and alpha1-beta2 isozymes, which are preferentially expressed in different regions of the inner ear and also with gastric and non-gastric H+/K+-ATPase.
VE:
1 * 100 µl
Artikel-Nr:
(SIALP64200-10G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
P64200-10G
Lokale Artikelnummer::
SIALP64200-10G
Beschreibung:
3,5-Pyridindicarbonsäure, Sigma-Aldrich®
VE:
1 * 10 g
Artikel-Nr:
(FLUO022642-1G)
Lieferant:
FLUOROCHEM
Hersteller-Artikelnummer::
022642-1G
Lokale Artikelnummer::
FLUO022642-1G
Beschreibung:
3,5-Dimethyl-p-anissäure
VE:
1 * 1 g
 This is a MarketSource item. Additional charges may apply
Lieferant:
Sigma-Aldrich
Beschreibung:
3,5-Difluorphenylboronsäure, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-8226R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8226R-A647
Lokale Artikelnummer::
BOSSBS-8226R-A647
Beschreibung:
FAM161B is a 647 amino acid protein that belongs to the FAM161 family. The gene that encodes FAM161B consists of approximately 16,413 bases and maps to human chromosome 14q24.3. Housing over 700 genes, chromosome 14 comprises nearly 3.5% of the human genome. Chromosome 14 encodes the Presenilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer’s disease. The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder α1-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction. An inversion of the long arm of chromosome 14 is thought to be involved in T-cell chronic lymphocytic leukemia (CLL), a cancer that affects T lymphocytes.
VE:
1 * 100 µl
Artikel-Nr:
(SIAL720410-1G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
720410-1G
Lokale Artikelnummer::
SIAL720410-1G
Beschreibung:
3,5-Dimethyl-4-isoxazolboronsäure, Sigma-Aldrich®
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-8260R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8260R-CY3
Lokale Artikelnummer::
BOSSBS-8260R-CY3
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-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8409R-CY7
Lokale Artikelnummer::
BOSSBS-8409R-CY7
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.
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noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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