You Searched For: SC-514

Catalog Number: (ENZOALX270427M005)

Supplier: ENZO LIFE SCIENCES

Description: Selective COX-1 inhibitor (IC50=9nM). Shows 700-fold more selectivity over COX-2 (IC50=6.3µM). Inhibits COX-1-derived platelet thromboxane B2, gastric PGE2, and dermal PGE2 production. Orally active in rat.

UOM: 1 * 5 mg

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Supplier: MACHEREY-NAGEL

Description: Filter paper, qualitative, Grade MN 514 ¹/₄, 320 mm

Supplier: AAT BIOQUEST

Description: IM7 is an anti-human/mouse monoclonal antibody that targets the CD44 antigen.

Supplier: AAT BIOQUEST

Description: UCHT2 is an anti-human monoclonal antibody that is specific for the CD5 antigen.

Supplier: AAT BIOQUEST

Description: 4H11 is an anti-human monoclonal antibody that recognises the CD34 antigen.

Catalog Number: (ENZOBMLRA1130025)

Supplier: ENZO LIFE SCIENCES

Description: Prostanoid receptor inhibitor

UOM: 1 * 25 mg

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Supplier: Biotium

Description: This MAb recognizes an extracellular epitope of an integral membrane glycoprotein of 150 kDa, identified as CD13. This antigen is present on most cells of myeloid origin including granulocytes, monocytes, mast cells, and GM-progenitor cells. It is also expressed by the majority of AML, CML in myeloid blast crisis, and in a smaller fraction of lymphoid leukemias. It is absent from normal lymphocytes, platelets and erythrocytes. CD13 is also present on fibroblasts; endothelial cells, epithelial cells from renal proximal tubules and intestinal brush border, bone marrow stromal cells, osteoclasts, and cells lining bile duct canaliculi. CD13 is identical to aminopeptidase N (APN), a prominent membrane-bound metalloprotease present on the surface of intestinal brush border and renal tubules. CD13 plays a role in metabolism of biologically active peptides, in phagocytosis, and in bactericidal/tumoricidal activities. It also serves as a receptor for human coronaviruses (HCV). The lineage-restricted pattern of expression of CD13 within the hemopoietic compartment suggests that it may be important in myeloid cell differentiation.

Supplier: BANDELIN-ELECTRONIC

Description: Ultrasonic bath accessories, Lid, D 514, stainless steel, For: SUPER RK 514 / H, DIGITEC DT 514 / H

Catalog Number: (BOSSBS-7740R-CY3)

Supplier: Bioss

Description: CCDC11 is a 514 amino acid protein encode by a gene that maps to human chromosome 18q21.1. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF∫ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18.

UOM: 1 * 100 µl

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Supplier: AAT BIOQUEST

Description: RPA-2.10 is an anti-human monoclonal antibody that is specific for the CD2 antigen.

Supplier: AAT BIOQUEST

Description: HIT2 is an anti-human monoclonal antibody that targets the CD38 antigen.

Catalog Number: (BRDY104554)

Supplier: Brady

Description: Extremely durable ToughStripe™ die-cut floor marking tapes are made of rugged polyester with an ultra-aggressive adhesive that will hold up against forklift traffic.

UOM: 1 * 1 Roll

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Catalog Number: (ROTH5008.1)

Supplier: Roth Carl

Description: Abietic acid

UOM: 1 * 25 g

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Supplier: AAT BIOQUEST

Description: SJ25C1 is an anti-human monoclonal antibody that forms an immune complex with the CD19 antigen.

Catalog Number: (BOSSBS-7740R-CY5)

Supplier: Bioss

Description: CCDC11 is a 514 amino acid protein encode by a gene that maps to human chromosome 18q21.1. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF∫ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18.

UOM: 1 * 100 µl

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Supplier: AAT BIOQUEST

Description: Anti-human secondary antibodies have well-characterised specificity for human immunoglobulins and are useful in the detection, sorting or purification of its specified target.

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