You Searched For: Molecular+sieve+3A+(0.3+nm,+3+Å)

Catalog Number: (7815200.)

Supplier: LABCONCO

Description: Solvent trap insert, contains molecular sieve, protects the rotary vane pump, For: Labconco CentriVap®

UOM: 1 * 1 items

Catalog Number: (634-0754)

Supplier: VWR Collection

Description: U-3900 and U-3900H spectrophotometers are comprehensive, research-grade solutions. They provide excellent performance afforded by low stray light, selectable band pass and high energy.

UOM: 1 * 1 items

Supplier: VWR Collection

Description: Reliable, accurate spectrophotometers for use in applications including biotechnology, material development and quality control.

Supplier: LABCONCO

Description: Molecular sieve replacement media, for drying trains

Supplier: APOLLO SCIENTIFIC

Description: BMS-309403 is an inhibitor of fatty acid binding protein 4 FABP4 with Ki of less than 2 nM that decreases fatty acid uptake in adipocytes in vitro.

Catalog Number: (SCOI285226010)

Supplier: SI Analytics

Description: Molecular sieve, 200 g in 250 ml glass bottle, TZ 1781

UOM: 1 * 1 items

Supplier: SGE Analytical Science

Description: Pure gas is a crictical requirement in gas chromatography, spectroscopy, optics, lithography and numerous other applications in manufacturing and laboratories. The SPure™ H₂O filters removes moisture, oil and dust from air and inert gases.

Supplier: Alfa Aesar

Description: AcroSeal™ septum bottled solvent.

Catalog Number: (661-1012)

Supplier: SI Analytics

Description: Starter kit KF, TZ 1789, consisting of molecular sieve, needles with syringes and glass wool, For: Titroline® 7750/7800

UOM: 1 * 1 items

Supplier: LABCONCO

Description: Radioisotope trap insert with molecular sieves for protecting the rotary vane vacuum pump (requires a clear PP canister with mounting bracket or stand for proper use), For: Labconco RapidVap®

Catalog Number: (BOSSBS-13280R-A680)

Supplier: Bioss

Description: The mammalian c-H-, c-K- and N-Ras proto-oncogenes encode ubiquitously expressed proteins (1,2). p21Ras can exist in either a physiologically quiescent GDP-binding state or a GTP-binding signal-emitting state (3). Oncogenic p21Ras proteins are trapped in the excited signal-emitting state because the mechanism normally employed to delimit their excitation period, hydrolysis of their bound GTP to GDP, is impaired as a result of specific mutations (3). Interaction of p21Ras with GTPase activating protein (GAP) can increase hydrolysis of p21Ras-bound GTP by as much as 1000-fold (4,5). The product of the neurofibromatosis type 1 gene (NF1) has also been shown to exhibit p21Ras GAP activity (6,7), and proteins that stimulate the GTPase activity of three other low molecular weight GTPases, including Rho, Rab 3A and Rap 1, have also been described (8,9).

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-13281R-CY5)

Supplier: Bioss

Description: The mammalian c-H-, c-K- and N-Ras proto-oncogenes encode ubiquitously expressed proteins (1,2). p21Ras can exist in either a physiologically quiescent GDP-binding state or a GTP-binding signal-emitting state (3). Oncogenic p21Ras proteins are trapped in the excited signal-emitting state because the mechanism normally employed to delimit their excitation period, hydrolysis of their bound GTP to GDP, is impaired as a result of specific mutations (3). Interaction of p21Ras with GTPase activating protein (GAP) can increase hydrolysis of p21Ras-bound GTP by as much as 1000-fold (4,5). The product of the neurofibromatosis type 1 gene (NF1) has also been shown to exhibit p21Ras GAP activity (6,7), and proteins that stimulate the GTPase activity of three other low molecular weight GTPases, including Rho, Rab 3A and Rap 1, have also been described (8,9).

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-13281R-CY7)

Supplier: Bioss

Description: The mammalian c-H-, c-K- and N-Ras proto-oncogenes encode ubiquitously expressed proteins (1,2). p21Ras can exist in either a physiologically quiescent GDP-binding state or a GTP-binding signal-emitting state (3). Oncogenic p21Ras proteins are trapped in the excited signal-emitting state because the mechanism normally employed to delimit their excitation period, hydrolysis of their bound GTP to GDP, is impaired as a result of specific mutations (3). Interaction of p21Ras with GTPase activating protein (GAP) can increase hydrolysis of p21Ras-bound GTP by as much as 1000-fold (4,5). The product of the neurofibromatosis type 1 gene (NF1) has also been shown to exhibit p21Ras GAP activity (6,7), and proteins that stimulate the GTPase activity of three other low molecular weight GTPases, including Rho, Rab 3A and Rap 1, have also been described (8,9).

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-13280R-CY7)

Supplier: Bioss

Description: The mammalian c-H-, c-K- and N-Ras proto-oncogenes encode ubiquitously expressed proteins (1,2). p21Ras can exist in either a physiologically quiescent GDP-binding state or a GTP-binding signal-emitting state (3). Oncogenic p21Ras proteins are trapped in the excited signal-emitting state because the mechanism normally employed to delimit their excitation period, hydrolysis of their bound GTP to GDP, is impaired as a result of specific mutations (3). Interaction of p21Ras with GTPase activating protein (GAP) can increase hydrolysis of p21Ras-bound GTP by as much as 1000-fold (4,5). The product of the neurofibromatosis type 1 gene (NF1) has also been shown to exhibit p21Ras GAP activity (6,7), and proteins that stimulate the GTPase activity of three other low molecular weight GTPases, including Rho, Rab 3A and Rap 1, have also been described (8,9).

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-13281R-A350)

Supplier: Bioss

Description: The mammalian c-H-, c-K- and N-Ras proto-oncogenes encode ubiquitously expressed proteins (1,2). p21Ras can exist in either a physiologically quiescent GDP-binding state or a GTP-binding signal-emitting state (3). Oncogenic p21Ras proteins are trapped in the excited signal-emitting state because the mechanism normally employed to delimit their excitation period, hydrolysis of their bound GTP to GDP, is impaired as a result of specific mutations (3). Interaction of p21Ras with GTPase activating protein (GAP) can increase hydrolysis of p21Ras-bound GTP by as much as 1000-fold (4,5). The product of the neurofibromatosis type 1 gene (NF1) has also been shown to exhibit p21Ras GAP activity (6,7), and proteins that stimulate the GTPase activity of three other low molecular weight GTPases, including Rho, Rab 3A and Rap 1, have also been described (8,9).

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-13281R-A680)

Supplier: Bioss

Description: The mammalian c-H-, c-K- and N-Ras proto-oncogenes encode ubiquitously expressed proteins (1,2). p21Ras can exist in either a physiologically quiescent GDP-binding state or a GTP-binding signal-emitting state (3). Oncogenic p21Ras proteins are trapped in the excited signal-emitting state because the mechanism normally employed to delimit their excitation period, hydrolysis of their bound GTP to GDP, is impaired as a result of specific mutations (3). Interaction of p21Ras with GTPase activating protein (GAP) can increase hydrolysis of p21Ras-bound GTP by as much as 1000-fold (4,5). The product of the neurofibromatosis type 1 gene (NF1) has also been shown to exhibit p21Ras GAP activity (6,7), and proteins that stimulate the GTPase activity of three other low molecular weight GTPases, including Rho, Rab 3A and Rap 1, have also been described (8,9).

UOM: 1 * 100 µl