cdna microarray abc human universochip 8k-1 (BioInnovations)
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cdna microarray abc human universochip 8k-1
Cdna Microarray Abc Human Universochip 8k 1, supplied by BioInnovations, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cdna+microarray+abc+human+universochip+8k-1/genomics+and+stem+cell+engineering/pm23184527-72-16-23
Average 90 stars, based on 1 article reviews
Cdna Microarray Abc Human Universochip 8k 1, supplied by BioInnovations, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cdna+microarray+abc+human+universochip+8k-1/genomics+and+stem+cell+engineering/pm23184527-72-16-23
Average 90 stars, based on 1 article reviews
cdna microarray abc human universochip 8k-1 - by Bioz Stars,
2026-09
90/100 stars
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Labeling:Article Title: Altered expression of carbonic anhydrase-related protein XI in neuronal cells expressing mutant ataxin-3. Article Snippet: Spinocerebellar ataxia type 3/Machado–Joseph disease (SCA3/MJD) is a late-onset neurodegenerative disorder caused by the expansion of a polyglutamine tract within the gene product, ataxin-3.. Microarray analysis revealed a dramatic differential expression of carbonic anhydraserelated protein XI (CA-RPXI/CA11) in the presence or absence of mutant ataxin-3.. Therefore, we examined the expression and distribution of all three CA-RPs (CA8, 10, and 11) in human neuronal cells that stably express mutant ataxin-3. Microarray:Article Title: Altered expression of carbonic anhydrase-related protein XI in neuronal cells expressing mutant ataxin-3. Article Snippet: Spinocerebellar ataxia type 3/Machado–Joseph disease (SCA3/MJD) is a late-onset neurodegenerative disorder caused by the expansion of a polyglutamine tract within the gene product, ataxin-3.. Microarray analysis revealed a dramatic differential expression of carbonic anhydraserelated protein XI (CA-RPXI/CA11) in the presence or absence of mutant ataxin-3.. Therefore, we examined the expression and distribution of all three CA-RPs (CA8, 10, and 11) in human neuronal cells that stably express mutant ataxin-3. Hybridization:Article Title: Altered expression of carbonic anhydrase-related protein XI in neuronal cells expressing mutant ataxin-3. Article Snippet: Spinocerebellar ataxia type 3/Machado–Joseph disease (SCA3/MJD) is a late-onset neurodegenerative disorder caused by the expansion of a polyglutamine tract within the gene product, ataxin-3.. Microarray analysis revealed a dramatic differential expression of carbonic anhydraserelated protein XI (CA-RPXI/CA11) in the presence or absence of mutant ataxin-3.. Therefore, we examined the expression and distribution of all three CA-RPs (CA8, 10, and 11) in human neuronal cells that stably express mutant ataxin-3. |