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Product Image-10155-492

Anti-DACH2 Rabbit Polyclonal Antibody

Catalog Number: (10155-492)
Supplier: Proteintech
Description: The DACH2 Antibody from Proteintech is a rabbit polyclonal Antibody to a fusion protein of human DACH2. This Antibody recognizes human, mouse Antigen. The DACH2 Antibody has been validated for the following applications: ELISA, WB analysis.
Product Image-10155-036

Anti-CPT1B Rabbit Polyclonal Antibody

Catalog Number: (10155-036)
Supplier: Proteintech
Description: The CPT1B-specific antibody from Proteintech is a rabbit polyclonal antibody to a fusion protein of human CPT1B-specific. This antibody recognizes human, mouse antigen. The CPT1B-specific antibody has been validated for the following applications: ELISA, WB analysis.
Product Image-10084-554

Anti-CDX2 Mouse Monoclonal Antibody [clone: 5A4E6]

Catalog Number: (10084-554)
Supplier: Proteintech
Description: CDX2, also named as Homeobox protein CDX-2, is a 313 amino acid protein, which contains one homeobox DNA-binding domain and belongs to the Caudal homeobox family. CDX2 localizes in the nucleus and is involved in the transcriptional regulation of multiple genes expression in the intestinal epithelium. The relative expression of CDX1 to CDX2 protein may be important in the anterior to posterior patterning of the intestinal epithelium and in defining patterns of proliferation and differentiation along the crypt-villus axis. Both Cdx1 and Cdx2 genes must be expressed to reduce tumorigenic potential, to increase sensitivity to apoptosis, and to reduce cell migration, suggesting that the two genes control the normal phenotype by independent pathways.
Image Unavailable-10428-856

Anti-C2CD3 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (10428-856)
Supplier: Bioss
Description: CA12 (Carbonic anhydrase XII) is a zinc metalloenzyme that catalyzes the reversible hydration of carbon dioxide.
Image Unavailable-10428-808

Anti-C2CD3 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10428-808)
Supplier: Bioss
Description: CA12 (Carbonic anhydrase XII) is a zinc metalloenzyme that catalyzes the reversible hydration of carbon dioxide.
Image Unavailable-10480-150

Anti-DHRS1 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10480-150)
Supplier: Bioss
Description: 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.
Image Unavailable-10480-154

Anti-DHRS1 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (10480-154)
Supplier: Bioss
Description: 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.
Image Unavailable-10480-156

Anti-DHRS1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (10480-156)
Supplier: Bioss
Description: 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.
Product Image-MSPP-100-1325

Human Recombinant Omentin

Catalog Number: (MSPP-100-1325)
Supplier: STEMCELL Technologies
Description: Use omentin for the maintenance of insulin sensitivity and metabolism, decreasing levels of this adipokine have been associated with obesity, insulin resistance, and diabetes (Tan <i>et al.</i>). Studies have suggested that omentin may have protective effects against atherosclerosis, arterial calcification, and myocardial injury through AMP-activated protein kinase (AMPK) and Akt-dependent mechanisms (Xu <i>et al.</i>, Kataoka <i>et al.</i>). Through regulation of Sirt1-dependent p53 deacetylation, omentin can inhibit proliferation and induce apoptosis in hepatocellular carcinoma cells (Zhang and Zhou). Omentin is mainly produced by visceral adipose tissue, but is also expressed in the small intestine, colon, mesothelial cells, vascular cells, and plasma (Watanabe et al). Protein sequence analysis has shown that omentin comprises 313 amino acids, with a secretory signal sequence and fibrinogen-related domain (Yang <i>et al.</i>). For consistency and reproducibility across your applications, Omentin from STEMCELL comes lyophilized with ≥90% purity, and is verified by LAL analysis to ensure endotoxin levels are ≤5,0 EU/μg protein.

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Image Unavailable-CAAA11047-03

Disodium hexachloroplatinate hexahydrate

Supplier: Thermo Scientific Chemicals
Description: Catalyst

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Image Unavailable-76120-286

Anti-C11orf65 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76120-286)
Supplier: Bioss
Description: C11orf65, also known as MGC33948, is a 313 amino acid protein that is encoded by a gene located on human chromosome 11. With 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' 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.
Product Image-10154-768

Anti-SPDYA Rabbit Polyclonal Antibody

Catalog Number: (10154-768)
Supplier: Proteintech
Description: The SPDYA Antibody from Proteintech is a rabbit polyclonal Antibody to a fusion protein of human SPDYA. This Antibody recognizes human,mouse,rat Antigen. The SPDYA Antibody has been validated for the following applications: ELISA, IP analysis.
Product Image-10787-302

Human Recombinant Omentin (from E. coli)

Supplier: FUJIFILM IRVINE SCIENTIFIC, INC
Description: Omentin is an adipokine that is produced and secreted by the small intestine, visceral adipose tissue, perivascular adipose tissue, and epicardial adipose tissue. Omentin enhances insulin-stimulated glucose uptake in adipocytes and is a link between obesity and Type 2 Diabetes. Omentin also functions as a vasodilator and plays a protective role during coronary atherosclerosis and hypertension.

Product Image-10154-818

Anti-PIGS Rabbit Polyclonal Antibody

Catalog Number: (10154-818)
Supplier: Proteintech
Description: The PIGS antibody from Proteintech is a rabbit polyclonal antibody to a fusion protein of human PIGS. This antibody recognizes human, mouse antigen. The PIGS antibody has been validated for the following applications: ELISA, WB, IF analysis.
Image Unavailable-75789-376

Human Recombinant CD87 (from Cells)

Catalog Number: (75789-376)
Supplier: Prosci
Description: The Urokinase Type Plasminogen Activator (uPA) receptor (uPAR) is a widely expressed receptor for urokinase plasminogen activator (uPA) and pro-uPA. uPAR / CD87 is a highly glycosylated, 55-60kDa integral membrane protein linked to the plasma membrane by a glycosylphosphatidylinositol (GPI) anchor. uPAR is expressed by T-cells, NK cells, monocytes, and neutrophils as well as non-hematopoietic cells that include vascular endothelial cells, fibroblasts, smooth muscle cells, keratinocytes, placental trophoblasts, hepatocytes, and a wide variety of tumor cells (including breast, colon, and prostate carcinoma, melanoma). It plays a critical role in the regulation of cell-surface plasminogen activation in physiological and pathological conditions, and it is also involved in cellular adhesion, the transmission of extracellular signals across the plasma membrane and the subsequent regulation of gene expression. uPAR has been implicated in several biological processes including angiogenesis, monocyte migration, cancer metastasis, trophoblast implantation, and wound healing. Human uPAR is encoded as a 313 amino acid residue polypeptide, excluding a 22 residue signal peptide and shows 60-70% similarity with the murine uPAR amino acid sequence although binding of uPA to uPAR shows strong species specificity.
Image Unavailable-76120-288

Anti-C11orf65 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (76120-288)
Supplier: Bioss
Description: C11orf65, also known as MGC33948, is a 313 amino acid protein that is encoded by a gene located on human chromosome 11. With 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' 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.
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
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