Print…

U heeft gezocht op: GEMINI+BIO-PRODUCTS


39 435  results were found

Verfijn resultaten Sorteren bij
SearchResultCount:"39435"

Sort Results

List view Easy View (new)

Rate These Search Results

Image Unavailable-BOSSBS-11563R-CY5

Anti-DDX20 Rabbit Polyclonal Antibody (Cy5®)

Catalogus nummer: (BOSSBS-11563R-CY5)
Leverancier: Bioss
Omschrijving: Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disease characterized by loss of motor neurons in the spinal cord. SMA is caused by deletion or loss-of-function mutations in the SMN (survival of motor neuron) gene. Gemin3, also known as DP103, DDX20, DEAD-box protein DP130 and DEAD/H box 20, is a protein product of human chromosome 1p13.2. It associates directly with SMN and is a part of the SMN complex containing Gemin2, Gemin4, Gemin5 and Gemin6, as well as several spliceosomal snRNP proteins. The SMN complex plays an essential role in spliceosomal snRNP assembly in the cytoplasm and is required for pre-mRNA splicing of the nucleus. It is found in both the cytoplasm and the nucleus. The nuclear form is concentrated in subnuclear bodies called gems (for Gemini of the coiled bodies). Gemin3 also interacts with SmB, SmD2 and SmD3. It contains the conserved motif Asp-Glu-Ala-Asp (DEAD) characteristic of DEAD-box proteins. Gemin3 is a putative RNA helicase and shows ATPase activity. It is expressed in B and T cell neuroblastoma-derived cell lines, malignant melanoma tumor, normal testis and is expressed in low levels in colon, skeletal muscle, liver, kidney and lung.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11563R-A647

Anti-DDX20 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalogus nummer: (BOSSBS-11563R-A647)
Leverancier: Bioss
Omschrijving: Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disease characterized by loss of motor neurons in the spinal cord. SMA is caused by deletion or loss-of-function mutations in the SMN (survival of motor neuron) gene. Gemin3, also known as DP103, DDX20, DEAD-box protein DP130 and DEAD/H box 20, is a protein product of human chromosome 1p13.2. It associates directly with SMN and is a part of the SMN complex containing Gemin2, Gemin4, Gemin5 and Gemin6, as well as several spliceosomal snRNP proteins. The SMN complex plays an essential role in spliceosomal snRNP assembly in the cytoplasm and is required for pre-mRNA splicing of the nucleus. It is found in both the cytoplasm and the nucleus. The nuclear form is concentrated in subnuclear bodies called gems (for Gemini of the coiled bodies). Gemin3 also interacts with SmB, SmD2 and SmD3. It contains the conserved motif Asp-Glu-Ala-Asp (DEAD) characteristic of DEAD-box proteins. Gemin3 is a putative RNA helicase and shows ATPase activity. It is expressed in B and T cell neuroblastoma-derived cell lines, malignant melanoma tumor, normal testis and is expressed in low levels in colon, skeletal muscle, liver, kidney and lung.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11563R-A555

Anti-DDX20 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Catalogus nummer: (BOSSBS-11563R-A555)
Leverancier: Bioss
Omschrijving: Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disease characterized by loss of motor neurons in the spinal cord. SMA is caused by deletion or loss-of-function mutations in the SMN (survival of motor neuron) gene. Gemin3, also known as DP103, DDX20, DEAD-box protein DP130 and DEAD/H box 20, is a protein product of human chromosome 1p13.2. It associates directly with SMN and is a part of the SMN complex containing Gemin2, Gemin4, Gemin5 and Gemin6, as well as several spliceosomal snRNP proteins. The SMN complex plays an essential role in spliceosomal snRNP assembly in the cytoplasm and is required for pre-mRNA splicing of the nucleus. It is found in both the cytoplasm and the nucleus. The nuclear form is concentrated in subnuclear bodies called gems (for Gemini of the coiled bodies). Gemin3 also interacts with SmB, SmD2 and SmD3. It contains the conserved motif Asp-Glu-Ala-Asp (DEAD) characteristic of DEAD-box proteins. Gemin3 is a putative RNA helicase and shows ATPase activity. It is expressed in B and T cell neuroblastoma-derived cell lines, malignant melanoma tumor, normal testis and is expressed in low levels in colon, skeletal muscle, liver, kidney and lung.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11563R-A680

Anti-Gemin 3/SMA Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalogus nummer: (BOSSBS-11563R-A680)
Leverancier: Bioss
Omschrijving: Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disease characterised by loss of motor neurons in the spinal cord. SMA is caused by deletion or loss-of-function mutations in the SMN (survival of motor neuron) gene. Gemin3, also known as DP103, DDX20, DEAD-box protein DP130 and DEAD/H box 20, is a protein product of human chromosome 1p13.2. It associates directly with SMN and is a part of the SMN complex containing Gemin2, Gemin4, Gemin5 and Gemin6, as well as several spliceosomal snRNP proteins. The SMN complex plays an essential role in spliceosomal snRNP assembly in the cytoplasm and is required for pre-mRNA splicing of the nucleus. It is found in both the cytoplasm and the nucleus. The nuclear form is concentrated in subnuclear bodies called gems (for Gemini of the coiled bodies). Gemin3 also interacts with SmB, SmD2 and SmD3. It contains the conserved motif Asp-Glu-Ala-Asp (DEAD) characteristic of DEAD-box proteins. Gemin3 is a putative RNA helicase and shows ATPase activity. It is expressed in B and T cell neuroblastoma-derived cell lines, malignant melanoma tumour, normal testis and is expressed in low levels in colon, skeletal muscle, liver, kidney and lung.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11563R-FITC

Anti-DDX20 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalogus nummer: (BOSSBS-11563R-FITC)
Leverancier: Bioss
Omschrijving: Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disease characterized by loss of motor neurons in the spinal cord. SMA is caused by deletion or loss-of-function mutations in the SMN (survival of motor neuron) gene. Gemin3, also known as DP103, DDX20, DEAD-box protein DP130 and DEAD/H box 20, is a protein product of human chromosome 1p13.2. It associates directly with SMN and is a part of the SMN complex containing Gemin2, Gemin4, Gemin5 and Gemin6, as well as several spliceosomal snRNP proteins. The SMN complex plays an essential role in spliceosomal snRNP assembly in the cytoplasm and is required for pre-mRNA splicing of the nucleus. It is found in both the cytoplasm and the nucleus. The nuclear form is concentrated in subnuclear bodies called gems (for Gemini of the coiled bodies). Gemin3 also interacts with SmB, SmD2 and SmD3. It contains the conserved motif Asp-Glu-Ala-Asp (DEAD) characteristic of DEAD-box proteins. Gemin3 is a putative RNA helicase and shows ATPase activity. It is expressed in B and T cell neuroblastoma-derived cell lines, malignant melanoma tumor, normal testis and is expressed in low levels in colon, skeletal muscle, liver, kidney and lung.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11563R-CY7

Anti-DDX20 Rabbit Polyclonal Antibody (Cy7®)

Catalogus nummer: (BOSSBS-11563R-CY7)
Leverancier: Bioss
Omschrijving: Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disease characterized by loss of motor neurons in the spinal cord. SMA is caused by deletion or loss-of-function mutations in the SMN (survival of motor neuron) gene. Gemin3, also known as DP103, DDX20, DEAD-box protein DP130 and DEAD/H box 20, is a protein product of human chromosome 1p13.2. It associates directly with SMN and is a part of the SMN complex containing Gemin2, Gemin4, Gemin5 and Gemin6, as well as several spliceosomal snRNP proteins. The SMN complex plays an essential role in spliceosomal snRNP assembly in the cytoplasm and is required for pre-mRNA splicing of the nucleus. It is found in both the cytoplasm and the nucleus. The nuclear form is concentrated in subnuclear bodies called gems (for Gemini of the coiled bodies). Gemin3 also interacts with SmB, SmD2 and SmD3. It contains the conserved motif Asp-Glu-Ala-Asp (DEAD) characteristic of DEAD-box proteins. Gemin3 is a putative RNA helicase and shows ATPase activity. It is expressed in B and T cell neuroblastoma-derived cell lines, malignant melanoma tumor, normal testis and is expressed in low levels in colon, skeletal muscle, liver, kidney and lung.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11563R-A750

Anti-Gemin 3/SMA Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalogus nummer: (BOSSBS-11563R-A750)
Leverancier: Bioss
Omschrijving: Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disease characterised by loss of motor neurons in the spinal cord. SMA is caused by deletion or loss-of-function mutations in the SMN (survival of motor neuron) gene. Gemin3, also known as DP103, DDX20, DEAD-box protein DP130 and DEAD/H box 20, is a protein product of human chromosome 1p13.2. It associates directly with SMN and is a part of the SMN complex containing Gemin2, Gemin4, Gemin5 and Gemin6, as well as several spliceosomal snRNP proteins. The SMN complex plays an essential role in spliceosomal snRNP assembly in the cytoplasm and is required for pre-mRNA splicing of the nucleus. It is found in both the cytoplasm and the nucleus. The nuclear form is concentrated in subnuclear bodies called gems (for Gemini of the coiled bodies). Gemin3 also interacts with SmB, SmD2 and SmD3. It contains the conserved motif Asp-Glu-Ala-Asp (DEAD) characteristic of DEAD-box proteins. Gemin3 is a putative RNA helicase and shows ATPase activity. It is expressed in B and T cell neuroblastoma-derived cell lines, malignant melanoma tumour, normal testis and is expressed in low levels in colon, skeletal muscle, liver, kidney and lung.
UOM: 1 * 100 µl
Image Unavailable-1.04057.2511

Glycerine 98.0-101.0% (by alkalimetry) Reag. Ph. Eur., ACS

Leverancier: Merck
Omschrijving: Bio-Based Glycerol
Our bio-based glycerol is produced from rapeseed, a renewable raw material, and a by-product of biodiesel production. It offers numerous advantages compared to petroleum-derived glycerol.

Certificaten Sale

Product Image-MLDVEM

Microplate reader, Gemini™ EM

Catalogus nummer: (MLDVEM)
Leverancier: Molecular Devices
Omschrijving: Gemini™ EM microplate spectrofluorometer provides a flexible environment to determine the optimal excitation and emission settings for most fluorescent intensity assays. The Gemini EM reader with dual monochromators allows researchers to try new and novel dyes without having to purchase expensive filter sets.
UOM: 1 * 1 ST
Image Unavailable-77067-5ML

Organic reference standard, Glycerol, analytical standard, Supelco®

Leverancier: Merck
Omschrijving: Glycerol may be used as a reference standard in the determination of glycerol in samples of beer using gas liquid chromatography (GLC). It is a simple polyol compound, which is obtained as a by-product of soap and bio-diesel industries. It is odourless, colour-less, viscous in nature, and exists as a sweet tasting liquid. It can be derived naturally as well as from petrochemical feedstock.
Glycerol has been used as:

Product Image-129-4034

VWR® Autoclave Bags, Polypropylene

Leverancier: VWR Collection
Omschrijving: <p>Sturdy, temperature resistant bags, ideal for disposing of non-hazardous waste or hazardous waste that must first be autoclaved. Can also be used for autoclaving other products. Supplied complete with wire closures that allow expansion of the bag and ventilation when cooling.</p>

Certificaten New Product

Product Image-MLDVXPS

Microplate readers, Gemini™ XPS

Catalogus nummer: (MLDVXPS)
Leverancier: Molecular Devices
Omschrijving: The Gemini™ XPS microplate spectrofluorometer provides a flexible environment to determine the optimal excitation and emission settings for most fluorescent intensity assays. The top reading Gemini™ XPS reader has dual monochromators that allow users to utilise new and novel dyes without purchasing expensive filter sets.
UOM: 1 * 1 ST
Product Image-1.10274.0001

Bioindicator, Sterikon® plus

Leverancier: Merck
Omschrijving: Sterikon® plus bio-indicatoren kunnen worden gebruikt om de functionaliteit van autoclaven te testen (15 minuten bij 121 °C). Ze kunnen ook worden gebruikt om elke soort autoclaaflading te controleren op het succes van sterilisatie. Bijvoorbeeld geneesmiddelen, met name producten in ampullen, ingeblikt voedsel enzovoort.

MSDS Certificaten

Product Image-735-0387

Optical bottom plates, SCREENSTAR

Leverancier: Greiner Bio-One
Omschrijving: Cycloolefin, black pigmented frame, 190 μm ultra-clear film bottom, tissue culture treated, sterile. SCREENSTAR microplates are specialised products for sophisticated microscopic applications, like high content screening (HCS) or high resolution microscopy with water and oil immersion objectives.

Environmentally Preferable

Image Unavailable-BOSSBS-11562R-HRP

Anti-GEMIN2 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalogus nummer: (BOSSBS-11562R-HRP)
Leverancier: Bioss
Omschrijving: Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disease characterized by loss of motor neurons in the spinal cord. SMA is caused by deletion or loss-of-function mutations in the SMN (survival of motor neuron) gene. Gemin2 (formerly known as SIP1 for SMN interacting protein) associates directly with SMN and is a part of the SMN complex containing Gemin3 (a DEAD-box RNA helicase), Gemin4, Gemin5 and Gemin6, as well as several spliceosomal snRNP proteins. The SMN complex plays an essential role in splicesomal snRNP assembly in the cytoplasm and is required for pre-mRNA splicing of the nucleus. It is found in both the cytoplasm and the nucleus. The nuclear form is concentrated in subnuclear bodies called gems (Gemini of the coiled bodies). The SMN-Gemin2 complex is associated with spliceosomal snRNAs U1 and U5. Gemin2 is expressed in spinal cord. It can be induced by TGF∫ treatment and expression is high in several E-cadherin negative human carcinoma cell lines. SMN is expressed in a wide variety of tissues including brain, kidney, liver and spinal cord, and moderately in skeletal and cardiac muscle. The gene encoding Gemin2 maps to human chromosome 14q13.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11562R-A350

Anti-GEMIN2 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Catalogus nummer: (BOSSBS-11562R-A350)
Leverancier: Bioss
Omschrijving: Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disease characterized by loss of motor neurons in the spinal cord. SMA is caused by deletion or loss-of-function mutations in the SMN (survival of motor neuron) gene. Gemin2 (formerly known as SIP1 for SMN interacting protein) associates directly with SMN and is a part of the SMN complex containing Gemin3 (a DEAD-box RNA helicase), Gemin4, Gemin5 and Gemin6, as well as several spliceosomal snRNP proteins. The SMN complex plays an essential role in splicesomal snRNP assembly in the cytoplasm and is required for pre-mRNA splicing of the nucleus. It is found in both the cytoplasm and the nucleus. The nuclear form is concentrated in subnuclear bodies called gems (Gemini of the coiled bodies). The SMN-Gemin2 complex is associated with spliceosomal snRNAs U1 and U5. Gemin2 is expressed in spinal cord. It can be induced by TGF∫ treatment and expression is high in several E-cadherin negative human carcinoma cell lines. SMN is expressed in a wide variety of tissues including brain, kidney, liver and spinal cord, and moderately in skeletal and cardiac muscle. The gene encoding Gemin2 maps to human chromosome 14q13.
UOM: 1 * 100 µl
Bel voor prijs
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
Dit artikel is geblokkeerd voor uw organisatie. Neem contact op met uw inkoopafdeling voor meer informatie
Het orginele artikel is niet langer beschikbaar. Het alternatief dat wordt getoond is beschikbaar
Product(en) gemarkeerd met dit symbool worden niet meer verkocht cq verkocht tot het einde van de voorraad. Alternatieven zijn mogelijk beschikbaar door te zoeken met het VWR-catalogusnummer dat hierboven wordt vermeld. Voor meer informatie kunt u contact opnemen met customer service: 020-4808410.
33 - 48 of 39 435
no targeter for Bottom