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Ataxin-1 Monoclonal Antibody, 100ul miRNA / siRNA Synthesis Defects in this gene are

SKU: 69073831154

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SEK135.00 SEK173.00

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Ataxin-1 Monoclonal Antibody, 100ul miRNA / siRNA Synthesis Defects in this gene areThe 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 genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always

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Description

Defects in this gene are associated with a susceptibility to asthma

Two related pseudogene have been identified on chromosomes 20 and X

The encoded protein is a negative regulator of NF-kappaB and can also sensitize cells to TNF- and TRAIL-induced apoptosis

The protein encoded by this gene associates with p300/CBP

The encoded protein (transcription factor AP-2 gamma) can act as either a homodimer or heterodimer with other family members and is induced during retinoic acid-mediated differentiation

Ataxin-1 Monoclonal Antibody, 100ul miRNA / siRNA Synthesis Defects in this gene areThe 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 genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always

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