You Searched For: 2,2,4-Trimethylpentane

Catalog Number: (BOSSBS-8336R)

Supplier: Bioss

Description: TMEM147, also known as ; NIFIE 14, is a 224 amino acid protein encoded by a gene mapping to human chromosome 19. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc?receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-8336R-A750)

Supplier: Bioss

Description: TMEM147, also known as ; NIFIE 14, is a 224 amino acid protein encoded by a gene mapping to human chromosome 19. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc?receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.

UOM: 1 * 100 µl

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Catalog Number: (BEST546W-10/XXL)

Supplier: Showa

Description: Featuring an engineered DURACoil liner and reinforced with HPPE, this cut- and abrasion-resistant model is an ultra-comfortable, multi-use work glove.

UOM: 1 * 10 PAIR

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Catalog Number: (BOSSBS-13132R-A555)

Supplier: Bioss

Description: FAHD1 is a 224 amino acid protein belonging to the FAH family. Present as a homodimer, FAHD1 is thought to have hydrolase activity and uses magnesium and calcium as cofactors. The gene that encodes FAHD1 maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, making up nearly 3% of human cellular DNA. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.

UOM: 1 * 100 µl

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Catalog Number: (44810.)

Supplier: Merck

Description: Organic Standard, Aroclor 1262 (PCB-mixture, 62% chlorinated) 1,000 µg/ml in isooctane

UOM: 1 * 1 items

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Catalog Number: (BOSSBS-13132R-A680)

Supplier: Bioss

Description: FAHD1 is a 224 amino acid protein belonging to the FAH family. Present as a homodimer, FAHD1 is thought to have hydrolase activity and uses magnesium and calcium as cofactors. The gene that encodes FAHD1 maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, making up nearly 3% of human cellular DNA. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-13132R-FITC)

Supplier: Bioss

Description: FAHD1 is a 224 amino acid protein belonging to the FAH family. Present as a homodimer, FAHD1 is thought to have hydrolase activity and uses magnesium and calcium as cofactors. The gene that encodes FAHD1 maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, making up nearly 3% of human cellular DNA. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.

UOM: 1 * 100 µl

Sale

Catalog Number: (BOSSBS-13132R-HRP)

Supplier: Bioss

Description: FAHD1 is a 224 amino acid protein belonging to the FAH family. Present as a homodimer, FAHD1 is thought to have hydrolase activity and uses magnesium and calcium as cofactors. The gene that encodes FAHD1 maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, making up nearly 3% of human cellular DNA. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.

UOM: 1 * 100 µl

Sale

Catalog Number: (BOSSBS-13132R-A350)

Supplier: Bioss

Description: FAHD1 is a 224 amino acid protein belonging to the FAH family. Present as a homodimer, FAHD1 is thought to have hydrolase activity and uses magnesium and calcium as cofactors. The gene that encodes FAHD1 maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, making up nearly 3% of human cellular DNA. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.

UOM: 1 * 100 µl

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Catalog Number: (SIMETC9224)

Supplier: Industrial Physics

Description: These single temperature indicating stickers are designed for use in electronics, food and pharmaceutical industries, and also in the oven and engine construction businesses. They are particularly useful for indicating temperatures of moving or inaccessible parts.

UOM: 1 * 50 items

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Catalog Number: (DELT232826)

Supplier: DELTALAB

Description: Made from recycled plastic. Suitable for a specific purpose and adapted to the demands of all types of healthcare and technical departments like treatment rooms and labs and technical facilities. One-handed disconnection. Strong handle for transporting.

UOM: 1 * 100 items

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Catalog Number: (44809.)

Supplier: Merck

Description: Organic Standard, Aroclor 1260 (PCB-mixture, 60% chlorinated) 1,000 µg/ml in isooctane

UOM: 1 * 1 items

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Catalog Number: (44808.)

Supplier: Merck

Description: Organic Standard, Aroclor 1254 (PCB-mixture, 54% chlorinated) 1,000 µg/ml in isooctane

UOM: 1 * 1 items

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Catalog Number: (510-4552)

Supplier: Retsch GmbH

Description: Sieves made from 304 stainless steel are individually laser engraved with clear and precise labelling for full traceability. Available in three of the most commonly used sizes. They are fully compatible with Retsch's existing products and can be combined with other sieves without problems.

UOM: 1 * 1 items

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Catalog Number: (115-1752)

Supplier: 3M

Description: These hand pads can be used in place of steel wool for conditioning metal surfaces and paint prep. Unlike fine steel wool, Scotch-Brite™ pads will not shred during use, rust after use, or leave fine metal splinters.

UOM: 1 * 20 items

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Supplier: NEXOPART

Description: These ALPINE air jet test sieves are suitable for fully automatic sieve recognition. These test sieves are made of brass/stainless steel frame with metal wire cloth made from stainless steel.