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Fournisseur:  Biotium
Description:   Recognizes a protein of 47-55 kDa, which is identified as FOXP3. Its precise epitope is not known, but it has been mapped to the N-terminal portion of the protein. The FOX family of transcription factors is a large group of proteins that share a common DNA binding domain termed a winged-helix or forkhead domain. During early development, FOXP1 and FOXP2 are expressed abundantly in the lung, with lower levels of expression in neural, intestinal and cardiovascular tissues, where they act as transcription repressors. FOXP1 is widely expressed in adult tissues, while neoplastic cells often exhibit a dramatic change in expression level or localization of FOXP1. Mutations in FOXP3 gene cause IPEX, a fatal, X-linked inherited disorder characterized by immune dysregulation. The FOXP3 protein is essential for normal immune homeostasis. Specifically, FOXP3 represses transcription through a DNA binding forkhead domain, thereby regulating T cell activation.
Fournisseur:  Biotium
Description:   Recognizes a protein of 47-55 kDa, which is identified as FOXP3. Its precise epitope is not known, but it has been mapped to the N-terminal portion (amino acids 2-136) of the protein.The FOX family of transcription factors is a large group of proteins that share a common DNA binding domain termed a winged-helix or forkhead domain. During early development, FOXP1 and FOXP2 are expressed abundantly in the lung, with lower levels of expression in neural, intestinal and cardiovascular tissues, where they act as transcription repressors. FOXP1 is widely expressed in adult tissues, while neoplastic cells often exhibit a dramatic change in expression level or localization of FOXP1. Mutations in FOXP3 gene cause IPEX, a fatal, X-linked inherited disorder characterized by immune dysregulation. The FOXP3 protein is essential for normal immune homeostasis. Specifically, FOXP3 represses transcription through a DNA binding forkhead domain, thereby regulating T cell activation.
Fournisseur:  Biotium
Description:   Recognizes a protein of 47-55 kDa, which is identified as FOXP3. Its precise epitope is not known, but it has been mapped to the N-terminal portion (amino acids 2-136) of the protein.The FOX family of transcription factors is a large group of proteins that share a common DNA binding domain termed a winged-helix or forkhead domain. During early development, FOXP1 and FOXP2 are expressed abundantly in the lung, with lower levels of expression in neural, intestinal and cardiovascular tissues, where they act as transcription repressors. FOXP1 is widely expressed in adult tissues, while neoplastic cells often exhibit a dramatic change in expression level or localization of FOXP1. Mutations in FOXP3 gene cause IPEX, a fatal, X-linked inherited disorder characterized by immune dysregulation. The FOXP3 protein is essential for normal immune homeostasis. Specifically, FOXP3 represses transcription through a DNA binding forkhead domain, thereby regulating T cell activation.
Fournisseur:  SGE a Trajan company
Description:   eVol® est la combinaison de deux éléments de précision: un entraînement électronique à lecture numérique et une seringue analytique XCHANGE®. Le résultat de cette combinaison est un système de distribution à déplacement positif avec contrôle numérique pouvant être programmé pour diverses procédures de traitement de liquides, reproductibles et précises.
Fournisseur:  Binder
Description:   The KBF series is a proven specialist for reliable ICH stability tests in the pharmaceutical industry: the KBF masters all long-term tests, accelerated tests and stress tests. It fulfills all important ICH requirements, from precision to programming and documentation. With flexible water supply options for all installation locations. The units have a stainless-steel inner chamber and proven APT.line™ preheating chamber technology, feature a temperature range of 0 to +70 °C, and humidity range of 10 to 80% RH, the KBF consumes up to 40 % less energy than its predecessor. With optional light modules, the KBF can be converted into an ICH photostability chamber and a plant growth chamber.
New Product
Numéro de catalogue: (BOSSBS-12549R-CY5)

Fournisseur:  Bioss
Description:   Vacuolar-type H+-ATPase (V-ATPase) is a multisubunit enzyme responsible for acidification of eukaryotic intracellular organelles. V-ATPases pump protons against an electrochemical gradient, while F-ATPases reverse the process, thereby synthesizing ATP. A peripheral V1 domain, which is responsible for ATP hydrolysis, and a integral V0 domain, which is responsible for proton translocation, compose V-ATPase. Nine subunits (A–H) make up the V1 domain and five subunits (a, d, c, c' and c") make up the V0 domain. Like F-ATPase, V-ATPase most likely operates through a rotary mechanism. The V-ATPase V1 B subunit exists as two isoforms. In the inner ear, the V-ATPase B1 isoform functions in proton secretion and is required to maintain proper endolymph pH and normal auditory function. The gene encoding the human V-ATPase B1 isoform maps to chromosome 2cen-q13. Mutations in this gene cause distal renal tubular acidosis associated with sensorineural deafness. The V-ATPase B2 isoform is expressed in kidney and is the only B isoform expressed in osteoclasts. The gene encoding the human V-ATPase B2 isoform maps to chromosome 8p22-p21.
UOM:  1 * 100 µl

Fournisseur:  VWR Collection
Description:   Cet instrument avec porte-électrodes articulé et boîtier de protection IP 43 offre une haute résolution et fiabilité pour des mesures précises. Sortie USB pour connexion à un ordinateur. Conforme aux BPL.
UOM:  1 * 1 SET
Fournisseur:  LABCONCO
Description:   Vacuum pump oil
Fournisseur:  Sartorius
Description:   Pipettes électroniques petites et légères qui réduisent la charge de travail de l'utilisateur, protègent l'utilisateur contre les blessures en assurant une posture de travail optimale et offrent des résultats de pipetage exacts et précis.
Fournisseur:  Restek
Description:   ASI replacement pump piston rods, Pour: Alliance® 2690
Numéro de catalogue: (224-0088)

Fournisseur:  GERBER FUNKE DR N.
Description:   Dosing Pump, Tête de pompe (accessoire pour pompe à tuyau), pour LactoStar
UOM:  1 * 1 ST
Numéro de catalogue: (BOSSBS-6038R-A350)

Fournisseur:  Bioss
Description:   A number of specific carrier proteins for members of the vitamin A family have been discovered. Cellular retinoic acid binding proteins (CRABP) are low molecular weight proteins whose precise function remains unknown. The inducibility of the CRABP2 gene suggests that this isoform is important in retinoic acid-mediated regulation of human skin growth and differentiation. It has been postulated that the CRABP2 gene is transcriptionally regulated by a newly synthesized regulatory protein.
UOM:  1 * 100 µl
Numéro de catalogue: (BOSSBS-6038R-A680)

Fournisseur:  Bioss
Description:   A number of specific carrier proteins for members of the vitamin A family have been discovered. Cellular retinoic acid binding proteins (CRABP) are low molecular weight proteins whose precise function remains unknown. The inducibility of the CRABP2 gene suggests that this isoform is important in retinoic acid-mediated regulation of human skin growth and differentiation. It has been postulated that the CRABP2 gene is transcriptionally regulated by a newly synthesised regulatory protein.
UOM:  1 * 100 µl
Numéro de catalogue: (BOSSBS-6038R-A750)

Fournisseur:  Bioss
Description:   A number of specific carrier proteins for members of the vitamin A family have been discovered. Cellular retinoic acid binding proteins (CRABP) are low molecular weight proteins whose precise function remains unknown. The inducibility of the CRABP2 gene suggests that this isoform is important in retinoic acid-mediated regulation of human skin growth and differentiation. It has been postulated that the CRABP2 gene is transcriptionally regulated by a newly synthesised regulatory protein.
UOM:  1 * 100 µl
Numéro de catalogue: (BOSSBS-1698R-CY5)

Fournisseur:  Bioss
Description:   Low-density lipoprotein (LDL) is the carrier protein for cholesterol in the blood. LDL binds to its receptor on the capillary walls and thereby mediates the uptake and clearence of cholesterol from the circulation. In atherosclerotic lesions oxidatively modified LDL is found and oxidized LDL is specifically recognized and ingested by macrophages via scavenger receptor A and CD36. Oxidized LDL may be a marker of atherosclerosis but the precise changes in oxidized LDL are not well described. Low-density lipoprotein oxidised with Cu2SO4.
UOM:  1 * 100 µl
Numéro de catalogue: (BOSSBS-1698R)

Fournisseur:  Bioss
Description:   Low-density lipoprotein (LDL) is the carrier protein for cholesterol in the blood. LDL binds to its receptor on the capillary walls and thereby mediates the uptake and clearence of cholesterol from the circulation. In atherosclerotic lesions oxidatively modified LDL is found and oxidized LDL is specifically recognized and ingested by macrophages via scavenger receptor A and CD36. Oxidized LDL may be a marker of atherosclerosis but the precise changes in oxidized LDL are not well described. Low-density lipoprotein oxidised with Cu2SO4.
UOM:  1 * 100 µl
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