You Searched For: \u03B1-Methylcinnamic+acid

Catalog Number: (GAINDFP-103C1-2WH)

Supplier: GA

Description: These thermoplastic waterproof labels are specifically designed to permanently adhere to vials, microcentrifuge tubes, microtubes, microplates, glass tubes, freezer boxes, plastic bags, and other specimen containers that will undergo long-term cryogenic and deep-freeze storage.

UOM: 1 * 1 Roll

Catalog Number: (BOSSBS-15090R-A488)

Supplier: Bioss

Description: Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf107 gene product has been provisionally designated C20orf107 pending further characterization.

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-15090R-HRP)

Supplier: Bioss

Description: Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf107 gene product has been provisionally designated C20orf107 pending further characterization.

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-15090R-A750)

Supplier: Bioss

Description: Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf107 gene product has been provisionally designated C20orf107 pending further characterization.

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-15090R-CY5)

Supplier: Bioss

Description: Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf107 gene product has been provisionally designated C20orf107 pending further characterization.

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-15090R-A680)

Supplier: Bioss

Description: Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf107 gene product has been provisionally designated C20orf107 pending further characterization.

UOM: 1 * 100 µl

Catalog Number: (KWIN853539940XL)

Supplier: FRISTADS KANSAS

Description: Industrial overall made of 65% polyester and 35% cotton, with soft nap on reverse side. The navy blue overall is available with different accent colours. The accent colour can be found on the top of the collar, on the inside front flap, on the pocket edges and and as a stripe on front and back.

UOM: 1 * 1 items

Supplier: Merck

Description: Suitable for general, non-critical laboratory applications or as a pretreatment for ultrapure water systems, the RiOs™ 3 system provides an ideal solution for Type III laboratory grade water needs such as manual cleaning and rinsing, buffer preparation, feed water for humidifiers, autoclaves and glassware washers. Designed for users seeking a compact, easy to use solution, the RiOs™ 3 system will be highly appreciated for its intuitive operation, small footprint and ease of maintenance. For users needing access to ultrapure water, the RiOs™ 3 system is ideal as pretreatment for Synergy® or Milli-Q® water purification systems. Up to 30 L/day of high quality analytical grade water (Type III water) from tap water.

Supplier: Alfa Aesar

Description: Cobalt(II) acetate tetrahydrate (24% Co)

Catalog Number: (DAIC87G35)

Supplier: CHIRAL TECHNOLOGIES

Description: These columns allow chromatographers to employ essentially any organic solvent as mobile phase to develop methods for the most challenging separations. These columns are available in a variety of particle sizes and offer great speed and column resolving power. Columns packed with 3 µm CSPs offer high speed separations and a reduction in analysis time and cost per sample. Columns, packed with 3 µm particles, may be used in conventional HPLC units without significant loss in performance, even with the smaller column dimensions.

UOM: 1 * 1 items

Catalog Number: (BOSSBS-15090R-FITC)

Supplier: Bioss

Description: Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf107 gene product has been provisionally designated C20orf107 pending further characterization.

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-9631R-A680)

Supplier: Bioss

Description: Involvement in disease; Defects in C16orf57 are the cause of poikiloderma with neutropenia (PN). PN is a genodermatosis characterised by poikiloderma, pachyonychia and chronic neutropenia. The disorder starts as a papular erythematous rash on the limbs during the first year of life. It gradually spreads centripetally and, as the papular rash resolves, hypo- and hyperpigmentation result, with development of telangiectasias. Another skin manifestation is pachyonychia, but alopecia and leukoplakia are distinctively absent. One of the most important extracutaneous symptoms is an increased susceptibility to infections, mainly affecting the respiratory system, primarily due to a chronic neutropenia and to neutrophil functional defects. Bone marrow abnormalities account for neutropenia and may evolve into myelodysplasia associated with the risk of leukemic transformation. Poikiloderma with neutropenia shows phenotypic overlap with Rothmund-Thomson syndrome.

UOM: 1 * 100 µl

Catalog Number: (SARBMCA2203S2S00-I)

Supplier: Sartorius Balances

Description: Cubis® II MCA precision balances with advanced user interface offer a maximum load of between 320 g and 14200 g and a readability of 1 to 100 mg provide, ideal model for every application.

UOM: 1 * 1 items

Catalog Number: (113-4847)

Supplier: FRISTADS KANSAS

Description: Overalls made from 65% polyester and 35% cotton, with soft nap on reverse side.

UOM: 1 * 1 items

Catalog Number: (BOSSBS-9631R-A750)

Supplier: Bioss

Description: Involvement in disease; Defects in C16orf57 are the cause of poikiloderma with neutropenia (PN). PN is a genodermatosis characterised by poikiloderma, pachyonychia and chronic neutropenia. The disorder starts as a papular erythematous rash on the limbs during the first year of life. It gradually spreads centripetally and, as the papular rash resolves, hypo- and hyperpigmentation result, with development of telangiectasias. Another skin manifestation is pachyonychia, but alopecia and leukoplakia are distinctively absent. One of the most important extracutaneous symptoms is an increased susceptibility to infections, mainly affecting the respiratory system, primarily due to a chronic neutropenia and to neutrophil functional defects. Bone marrow abnormalities account for neutropenia and may evolve into myelodysplasia associated with the risk of leukemic transformation. Poikiloderma with neutropenia shows phenotypic overlap with Rothmund-Thomson syndrome.

UOM: 1 * 100 µl

Catalog Number: (113-4831)

Supplier: FRISTADS KANSAS

Description: Overalls made from 65% polyester and 35% cotton, with soft nap on reverse side.

UOM: 1 * 1 items