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ATXN1 blocking peptide

ATXN1 Immunizing Peptide

Gene Names
ATXN1; ATX1; SCA1; D6S504E
Reactivity
Human, Dog, Pig
Synonyms
ATXN1; ATXN1 Immunizing Peptide; ataxin 1; ATX1; D6S504E; SCA1; OTTHUMP00000016065; OTTHUMP00000039306; olivopontocerebellar ataxia 1; autosomal dominant; spinocerebellar ataxia 1 (olivopontocerebellar ataxia 1; ataxin 1); ATXN1 blocking peptide
Ordering
For Research Use Only!
Reactivity
Human, Dog, Pig
Form/Format
100ug of dried peptide
Sequence
C-DLEVQQATHREASP
Sequence Length
815
Preparation and Storage
Shipped at ambient temperature, store at -20 degree C

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
Molecular Weight
86,923 Da
NCBI Official Full Name
ataxin-1
NCBI Official Synonym Full Names
ataxin 1
NCBI Official Symbol
ATXN1
NCBI Official Synonym Symbols
ATX1; SCA1; D6S504E
NCBI Protein Information
ataxin-1
UniProt Protein Name
Ataxin-1
Protein Family
UniProt Gene Name
ATXN1
UniProt Synonym Gene Names
ATX1; SCA1
UniProt Entry Name
ATX1_HUMAN

NCBI Description

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 genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the `pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders. Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions. ADCA is caused by the expansion of the CAG repeats, producing an elongated polyglutamine tract in the corresponding protein. The expanded repeats are variable in size and unstable, usually increasing in size when transmitted to successive generations. The function of the ataxins is not known. This locus has been mapped to chromosome 6, and it has been determined that the diseased allele contains 41-81 CAG repeats, compared to 6-39 in the normal allele, and is associated with spinocerebellar ataxia type 1 (SCA1). At least two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jan 2010]

Uniprot Description

ataxin-1: spinocerebellar ataxia type 1 (SCA1) protein. Expansion of CAG repeats in the SCA1 gene results in an abnormally long polyglutamine tract in the protein, causing polyglutamine-induced neurodegeneration. 14-3-3 and Akt kinase stabilize both wild-type and mutant forms of ataxin-1. The expansion of the polyglutamine tract may alter this function.

Protein type: RNA-binding; Nuclear export

Chromosomal Location of Human Ortholog: 6p23

Cellular Component: cytoplasm; intracellular membrane-bound organelle; nuclear inclusion body; nuclear matrix; nuclear RNA export factor complex; nucleoplasm; nucleus

Molecular Function: DNA binding; identical protein binding; poly(rG) binding; poly(U) binding; protein binding; protein C-terminus binding; protein self-association

Biological Process: negative regulation of transcription, DNA-dependent; nuclear export; RNA processing; transcription, DNA-dependent

Disease: Spinocerebellar Ataxia 1

Research Articles on ATXN1

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Product Notes

The ATXN1 atxn1 (Catalog #AAA428496) is a Blocking Peptide and is intended for research purposes only. The product is available for immediate purchase. The ATXN1 Immunizing Peptide reacts with Human, Dog, Pig and may cross-react with other species as described in the data sheet. The amino acid sequence is listed below: C-DLEVQQAT HREASP. It is sometimes possible for the material contained within the vial of "ATXN1, Blocking Peptide" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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