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Image Unavailable-TCF1235-25MG

RITA ≥98.0% (by GC)

Supplier: TCI America
Description: RITA ≥98.0% (by GC)

New Product

Product Image-89151-254

RITA ≥98%

Catalog Number: (89151-254)
Supplier: Enzo Life Sciences
Description: Inhibitor of p53/HDM2 interaction
Image Unavailable-77686-193

RITA 98%

Supplier: Ambeed
Description: RITA 98%

New Product

Image Unavailable-AAJ65379-MA

RITA

Catalog Number: (AAJ65379-MA)
Supplier: Thermo Scientific Chemicals
Description: A cell-permeable, p53-targeting, tricyclic thiophene derivative

SDS Certificates


Image Unavailable-103285-266

Anti-RITA Rabbit Polyclonal Antibody

Catalog Number: (103285-266)
Supplier: Novus Biologicals
Description: The RITA Antibody from Novus Biologicals is a rabbit polyclonal antibody to RITA. This antibody reacts with human. The RITA Antibody has been validated for the following applications: Immunohistochemistry, Immunohistochemistry-Paraffin.
Image Unavailable-10268-612

Anti-RITA/C12orf52 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (10268-612)
Supplier: Bioss
Description: Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf52 gene product has been provisionally designated C12orf52 pending further characterization.
Image Unavailable-10268-594

Anti-RITA/C12orf52 Rabbit Polyclonal Antibody

Catalog Number: (10268-594)
Supplier: Bioss
Description: Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf52 gene product has been provisionally designated C12orf52 pending further characterization.
Image Unavailable-10268-614

Anti-RITA/C12orf52 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (10268-614)
Supplier: Bioss
Description: Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf52 gene product has been provisionally designated C12orf52 pending further characterization.
Product Image-76010-856

Anti-RITA1 Rabbit Polyclonal Antibody

Catalog Number: (76010-856)
Supplier: Prosci
Description: For WB starting dilution is: 1:1000
Image Unavailable-10268-610

Anti-RITA1 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (10268-610)
Supplier: Bioss
Description: Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf52 gene product has been provisionally designated C12orf52 pending further characterization.
Image Unavailable-10268-606

Anti-RITA1 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (10268-606)
Supplier: Bioss
Description: Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf52 gene product has been provisionally designated C12orf52 pending further characterization.
Image Unavailable-10268-608

Anti-RITA1 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10268-608)
Supplier: Bioss
Description: Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf52 gene product has been provisionally designated C12orf52 pending further characterization.
Image Unavailable-102871-002

RITA (1 MG)

Catalog Number: (102871-002)
Supplier: R&D Systems
Description: RITA (1 MG)
Image Unavailable-102871-004

RITA (10 MG)

Catalog Number: (102871-004)
Supplier: R&D Systems
Description: RITA (10 MG)
Image Unavailable-101366-042

P53 ACTIVATOR III RITA-1MG

Catalog Number: (101366-042)
Supplier: MilliporeSigma
Description: P53 ACTIVATOR III RITA-1MG

Certificates


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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
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