- Search results for O15265
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10 products were found matching "O15265"!
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Item number: A302-638A
Protein function: Acts as component of the STAGA transcription coactivator-HAT complex. Mediates the interaction of STAGA complex with the CRX and is involved in CRX-dependent gene activation. Necessary for microtubule cytoskeleton stabilization. [The UniProt Consortium]
Keywords: | Anti-SCA7, Anti-ATXN7, Anti-Ataxin-7, Anti-Spinocerebellar ataxia type 7 protein |
Application: | WB, IP |
Host: | Rabbit |
Species reactivity: | human |
From 164.00€
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Item number: E-AB-53584.120
The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five...
Keywords: | Anti-SCA7, Anti-ATXN7, Anti-Ataxin-7, Anti-Spinocerebellar ataxia type 7 protein, ATXN7 Polyclonal Antibody |
Application: | IHC, ELISA |
Host: | Rabbit |
Species reactivity: | human, mouse |
From 71.00€
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Item number: G-PACO55402.50
ATXN7 Antibody is a IgG polyclonal antibody from Assay Genie with reactivity against Human, Rat and for use in ELISA, WB, IHC, IF applications. ATXN7 Antibody is a high quality polyclonal antibody for research use only.. Protein function: Acts as component of the STAGA transcription coactivator-HAT complex. Mediates...
Keywords: | Anti-SCA7, Anti-ATXN7, Anti-Ataxin-7, Anti-Spinocerebellar ataxia type 7 protein |
Application: | ELISA, WB, IHC, IF |
Host: | Rabbit |
Species reactivity: | human, rat |
363.00€
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Item number: ELK-ES9411.100
ataxin 7(ATXN7) Homo sapiens The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically...
Keywords: | Anti-ATXN7, Anti-Ataxin-7, Anti-Spinocerebellar ataxia type 7 protein, ATX7 rabbit pAb |
Application: | WB, ELISA |
Host: | Rabbit |
Species reactivity: | human, mouse |
From 169.00€
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Item number: 032320-APC.200
The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five...
Application: | FLISA, WB |
Host: | Rabbit |
Species reactivity: | human |
993.00€
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Item number: 032320-Biotin.200
The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five...
Application: | ELISA, WB |
Host: | Rabbit |
Species reactivity: | human |
993.00€
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Item number: 032320-FITC.200
The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five...
Application: | FLISA, WB |
Host: | Rabbit |
Species reactivity: | human |
993.00€
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Item number: 032320-HRP.200
The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five...
Application: | ELISA, WB |
Host: | Rabbit |
Species reactivity: | human |
993.00€
*
Item number: 032320.200
The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five...
Keywords: | Anti-SCA7, Anti-ATXN7, Anti-Ataxin-7, Anti-Spinocerebellar ataxia type 7 protein |
Application: | ELISA, WB |
Host: | Rabbit |
Species reactivity: | human |
728.00€
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Item number: A4159-16.100
Ataxin-7 is a protein of unknown function. However, since this protein contains a nuclear localization sequence and is found to be localized in the nucleus, it has been postulated to be a potential transcription factor. Spinocerebellar ataxia-7 (one of a group of hereditary neurodegenrative diseases) is caused by an...
Keywords: | Anti-SCA7, Anti-Spinocerebellar ataxia type 7 protein |
Application: | WB |
Host: | Mouse |
Species reactivity: | human, mouse, rat |
826.00€
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