You Searched For: borne

Catalog Number: (APOSBITP1928-1MG)

Supplier: Apollo Scientific

Description: Recombinant Tick-Borne Encephalitis Virus preM

UOM: 1 * 1 mg

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Catalog Number: (APOSBITP1926-1MG)

Supplier: Apollo Scientific

Description: Recombinant Tick-Borne Encephalitis Virus Core

UOM: 1 * 1 mg

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Catalog Number: (APOSBITP1927-1MG)

Supplier: Apollo Scientific

Description: Recombinant Tick-Borne Encephalitis Virus NS3

UOM: 1 * 1 mg

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Catalog Number: (APOSBITP1923-1MG)

Supplier: Apollo Scientific

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

UOM: 1 * 1 mg

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Catalog Number: (APOSBITP1924-1MG)

Supplier: Apollo Scientific

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

UOM: 1 * 1 mg

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Catalog Number: (APOSBITP1920-1MG)

Supplier: Apollo Scientific

Description: Recombinant Tick-Borne Encephalitis Virus NE/gE

UOM: 1 * 1 mg

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Catalog Number: (APOSBITP1919-1MG)

Supplier: Apollo Scientific

Description: Recombinant Tick-Borne Encephalitis Virus gE

UOM: 1 * 1 mg

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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

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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.

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Catalog Number: (BOSSBS-4192R-CY3)

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

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Catalog Number: (BOSSBS-4192R)

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

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Catalog Number: (BOSSBS-12356R-CY7)

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

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Catalog Number: (BOSSBS-12356R-FITC)

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

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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

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Catalog Number: (BOSSBS-4192R-A680)

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

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Catalog Number: (BOSSBS-4192R-A647)

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

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