You Searched For: bra30

Catalog Number: (10785-332)

Supplier: CHI Scientific

Description: The PrimaCell™ system has been developed for the acquisition and growth of primary cells from a variety of different tissue types. Each PrimaCell™ kit has been optimized for each cell type to produce 4-7 times the number of primary cells obtained from published literature protocols. Each kit comes with 100 ml of tissue washing medium, our optimized tissue dissociation system OptiTDS™, 500 ml of growth medium, and enough growth supplements and serum to add to the supplied medium. Kits that require a Fibroblast control system also come with our FibrOut™ kit (added to the growth medium) which reduces or eliminates Fibroblast growth after 2-3 cell growth cycles.

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Catalog Number: (89322-256)

Supplier: Genetex

Description: Protein extract from Human Brain: Occipital Lobe (Multiple Sclerosis) Pkg Size: 200 ug

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Catalog Number: (89322-288)

Supplier: Genetex

Description: Protein extract from Human Brain: Corpus Callosum (Multiple Sclerosis) Pkg Size: 200 ug

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Catalog Number: (10265-752)

Supplier: Bioss

Description: MPPED2 (Metallophosphoesterase domain-containing protein 2), also known as C11orf8, FAM1B or 239FB, is a 294 amino acid protein. Expressed primarily in fetal brain tissue, MPPED2 is encoded by a gene that maps to chromosome 11. 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 stranded 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, while 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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Catalog Number: (10265-754)

Supplier: Bioss

Description: MPPED2 (Metallophosphoesterase domain-containing protein 2), also known as C11orf8, FAM1B or 239FB, is a 294 amino acid protein. Expressed primarily in fetal brain tissue, MPPED2 is encoded by a gene that maps to chromosome 11. 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 stranded 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, while 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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Supplier: VWR

Description: Ward’s® PURE Preserved Specimens - the best dissection experience from start to finish.

Catalog Number: (10265-750)

Supplier: Bioss

Description: MPPED2 (Metallophosphoesterase domain-containing protein 2), also known as C11orf8, FAM1B or 239FB, is a 294 amino acid protein. Expressed primarily in fetal brain tissue, MPPED2 is encoded by a gene that maps to chromosome 11. 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 stranded 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, while 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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Catalog Number: (89322-208)

Supplier: Genetex

Description: Protein extract from Human Brain: Temporal Lobe (Progressive Supranuclear Palsy) Pkg Size: 200 ug

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Catalog Number: (10265-748)

Supplier: Bioss

Description: MPPED2 (Metallophosphoesterase domain-containing protein 2), also known as C11orf8, FAM1B or 239FB, is a 294 amino acid protein. Expressed primarily in fetal brain tissue, MPPED2 is encoded by a gene that maps to chromosome 11. 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 stranded 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, while 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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Catalog Number: (89322-240)

Supplier: Genetex

Description: Protein extract from Human Brain: Parietal Lobe (Progressive Supranuclear Palsy) Pkg Size: 200 ug

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Catalog Number: (89322-252)

Supplier: Genetex

Description: Protein extract from Human Brain: Occipital Lobe (Progressive Supranuclear Palsy) Pkg Size: 200 ug

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Supplier: CHI Scientific

Description: Kit PrimaCell* 10 Human Brain OptiTDS* 10, Tissue Dissociation System, Stability, package should be stored at -20 degree C, effective up to 4 months

Catalog Number: (89322-264)

Supplier: Genetex

Description: Protein extract from Human Brain: Medulla oblongata (Progressive Supranuclear Palsy) Pkg Size: 200 ug

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Catalog Number: (89322-274)

Supplier: Genetex

Description: Protein extract from Human Brain: Frontal Lobe (Progressive Supranuclear Palsy) Pkg Size: 200 ug

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Supplier: CHI Scientific

Description: Kit PrimaCell* 10 Mouse Brain OptiTDS* 10: Tissue Dissociation System, stable for 7-10 days at 4 C. The unused kit is stable and effective up to 6 months at the -20 C.

Catalog Number: (10783-218)

Supplier: CHI Scientific

Description: The PrimaCell™ system has been developed for the acquisition and growth of primary cells from a variety of different tissue types. Each PrimaCell™ kit has been optimized for each cell type to produce 4-7 times the number of primary cells obtained from published literature protocols. Each kit comes with 100 ml of tissue washing medium, our optimized tissue dissociation system OptiTDS™, 500 ml of growth medium, and enough growth supplements and serum to add to the supplied medium. Kits that require a Fibroblast control system also come with our FibrOut™ kit (added to the growth medium) which reduces or eliminates Fibroblast growth after 2-3 cell growth cycles.

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