You Searched For: borne

Catalog Number: (APOSBITP1926-1MG)

Supplier: Apollo Scientific

Description: Recombinant Tick-Borne Encephalitis Virus Core

UOM: 1 * 1 mg

Sale

Catalog Number: (APOSBITP1928-1MG)

Supplier: Apollo Scientific

Description: Recombinant Tick-Borne Encephalitis Virus preM

UOM: 1 * 1 mg

Sale

Catalog Number: (APOSBITP1924-1MG)

Supplier: Apollo Scientific

Description: Recombinant Tick-Borne Encephalitis Virus gE C-end (296-414)

UOM: 1 * 1 mg

Sale

Catalog Number: (APOSBITP1923-1MG)

Supplier: Apollo Scientific

Description: Recombinant Tick-Borne Encephalitis Virus gE middle (50-250)

UOM: 1 * 1 mg

Sale

Catalog Number: (APOSBITP1920-1MG)

Supplier: Apollo Scientific

Description: Recombinant Tick-Borne Encephalitis Virus NE/gE

UOM: 1 * 1 mg

Sale

Catalog Number: (APOSBITP1927-1MG)

Supplier: Apollo Scientific

Description: Recombinant Tick-Borne Encephalitis Virus NS3

UOM: 1 * 1 mg

Sale

Catalog Number: (APOSBITP1919-1MG)

Supplier: Apollo Scientific

Description: Recombinant Tick-Borne Encephalitis Virus gE

UOM: 1 * 1 mg

Sale

Supplier: ENZO LIFE SCIENCES

Description: Sulfur containing antibiotic. Potent inhibitor of bacterial and yeast RNA polymerases. Inhibits mRNA chain elongation. Inhibits adhesion of endothelial cells (HUVECs) to vitronectin (IC50=0.83 µM) thereby inhibiting tumor cell-induced angiogenesis in vivo. Inhibits transcription in C. albicans. Inhibits microbiological growth in beer. Active against soil borne pathogens.

New Product

Catalog Number: (BOSSBS-4192R-FITC)

Supplier: Bioss

Description: SLC25A20 is one of several closely related mitochondrial membrane carrier proteins that shuttle substrates between cytosol and the intramitochondrial matrix space. It mediates the transport of acylcarnitines into the mitochondrial matrix for their oxidation by the mitochondrial fatty acid oxidation pathway. Mutations in this gene are associated with carnitine acylcarnitine translocase deficiency, which can cause a variety of pathological conditions such as hypoglycemia, cardiac arrest, hepatomegaly, hepatic dysfunction and muscle weakness, and is usually lethal in new born and infants.

UOM: 1 * 100 µl

Sale

Catalog Number: (BOSSBS-4192R-A488)

Supplier: Bioss

Description: SLC25A20 is one of several closely related mitochondrial membrane carrier proteins that shuttle substrates between cytosol and the intramitochondrial matrix space. It mediates the transport of acylcarnitines into the mitochondrial matrix for their oxidation by the mitochondrial fatty acid oxidation pathway. Mutations in this gene are associated with carnitine acylcarnitine translocase deficiency, which can cause a variety of pathological conditions such as hypoglycemia, cardiac arrest, hepatomegaly, hepatic dysfunction and muscle weakness, and is usually lethal in new born and infants.

UOM: 1 * 100 µl

Sale

Catalog Number: (BOSSBS-4192R-A555)

Supplier: Bioss

Description: SLC25A20 is one of several closely related mitochondrial membrane carrier proteins that shuttle substrates between cytosol and the intramitochondrial matrix space. It mediates the transport of acylcarnitines into the mitochondrial matrix for their oxidation by the mitochondrial fatty acid oxidation pathway. Mutations in this gene are associated with carnitine acylcarnitine translocase deficiency, which can cause a variety of pathological conditions such as hypoglycemia, cardiac arrest, hepatomegaly, hepatic dysfunction and muscle weakness, and is usually lethal in new born and infants.

UOM: 1 * 100 µl

Sale

Catalog Number: (BOSSBS-12356R)

Supplier: Bioss

Description: ALX1 is a 326 amino acid protein specific to cervix and cartilage tissues. As well as having a homeobox domain, ALX1 also contains an OAR domain, which has been suggested to be important for DNA binding or protein-protein interactions and transactivation. First characterized from a rat chondrosarcoma tumor cell line, ALX1 is a homeobox transcription factor that regulates downstream target genes and has specifically shown to act as a transcriptional repressor for rat prolactin in vivo. Homozygous ALX1 deficient mice are born with acrania and meroanencephaly, suggesting ALX1 function in the development of the neural tube. It has also been suggested that ALX1 cooperates with ALX4 in limb development and craniofacial bone formation.

UOM: 1 * 100 µl

Sale

Catalog Number: (BOSSBS-12356R-A350)

Supplier: Bioss

Description: ALX1 is a 326 amino acid protein specific to cervix and cartilage tissues. As well as having a homeobox domain, ALX1 also contains an OAR domain, which has been suggested to be important for DNA binding or protein-protein interactions and transactivation. First characterized from a rat chondrosarcoma tumor cell line, ALX1 is a homeobox transcription factor that regulates downstream target genes and has specifically shown to act as a transcriptional repressor for rat prolactin in vivo. Homozygous ALX1 deficient mice are born with acrania and meroanencephaly, suggesting ALX1 function in the development of the neural tube. It has also been suggested that ALX1 cooperates with ALX4 in limb development and craniofacial bone formation.

UOM: 1 * 100 µl

Sale

Supplier: KIMBERLY CLARK

Description: Transparent black, portable, single-sheet wiper dispenser. Ensures rolls remain clean and enclosed to help prevent transmission of food-borne bacteria. Fits service and retail centrefeed rolls (115-2527) and food and hygiene centrefeed rolls (115-2529 and 115-2531).

Supplier: VWR Collection

Description: B'mat decontamination flooring uses a patented polymer to attract and retain over 98% of foot- and wheel-borne particles. Particles are naturally attracted by the flooring surface, and are released only by wet cleaning. This flooring needs to be glued to the floor, which ensures a perfect hold and maximum lifespan. Ideal solution for contamination control in gowning areas, in material entry zones, and in cleanrooms.

New Product

Catalog Number: (BOSSBS-7856R-CY5)

Supplier: Bioss

Description: Introduces molecular oxygen into polyunsaturated fatty acids. Exact substrate is not known.Tissue specificity:Predominantly expressed in skin.Involvement in diseaseDefects in ALOXE3 are a cause of non-bullous congenital ichthyosiform erythroderma (NCIE). NCIE is a non-bullous ichthyosis, a skin disorder characterized by abnormal cornification of the epidermis. Most affected individuals are born with a tight, shiny, translucent covering called collodion membrane. The collodion membrane subsequently evolves into generalized scaling and intense redness of the skin. Clinical features are milder than in lamellar ichthyoses and demonstrate a greater variability in the intensity of erythema, size and type of scales. In contrast to lamellar ichthyoses, scales are usually white, fine and powdery, and palms and soles are severely affected. Patients suffer from palmoplantar keratoderma, often with painful fissures, digital contractures, and loss of pulp volume.

UOM: 1 * 100 µl

Sale