ATXN1 (Ser775) Antibody

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Catalog number: bs-3008R
Price: 281 €
Supplier: Bioss Primary Unconjugated Antibodies
Product name: ATXN1 (Ser775) Antibody
Quantity: 0.1ml
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Long name: ATXN1 (Ser775) Primary Polyclonal Antibody
Also known as: ATXN1 (Ser775) PAb
Category: Primary Antibodies
Conjugation: Unconjugated
Target Antigen: ATXN1 Ser775
Specificity: This is a highly specific antibody against ATXN1 Ser775
Modification(s): Phosphorylation
Modification site(s): Ser775
Clonality: Polyclonal antibody
Clone number: Polyclonal antibody
Concentration: 1ug per 1ul
Source: KLH conjugated synthetic phosphopeptide derived from human Ataxin-1 around the phosphorylation site of Ser775
Gene ID number: 6310
Tested Applications: IF(IHC-P), IHC-P, WB
Recommended dilutions: IF(IHC-P)(1:50-200), IHC-P(1:100-500), WB(1:100-1000)
Cross reactivity: Mouse, Rat, Human
Cross reactive species details: not every possible cross-reactivity is known, Due to limited amount of testing and knowledge
Background of the target antigen: 2, 3, 4 and 6, ADCA has been divided into three groups: ADCA types I-III, ADCA is caused by the expansion of the CAG repeats, ADCAI is genetically heterogeneous, ADCAII, At least two transcript variants encoding the same protein have been found for this gene, Clinically, Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions, The expanded repeats are variable in size and unstable, The function of the ataxins is not known, This locus has been mapped to chromosome 6, [provided by RefSeq], and ADCAIII often referred to as the `pure' cerebellar syndrome (SCA5), and is associated with spinocerebellar ataxia type 1 (SCA1), and it has been determined that the diseased allele contains41-81 CAG repeats, are most likely homogeneous disorders, being assigned to five different chromosomes, brain stem and spinal cord, compared to 6-39 in the normal allele, designated spinocerebellar ataxia (SCA) 1, producing an elongated polyglutamine tract in the corresponding protein, usually increasing in size when transmitted to successive generations, which always presents with retinal degeneration (SCA7), with five genetic loci, The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum
Purification method: This antibody was purified via Protein A
Storage conditions: 50% glycerol and 0, Store at -20°, 09% sodium azide, C for up to 1 year, Keep the antibody in aqueous buffered solution containing 1% BSA
Synonym names: ATX1, ATX1_HUMAN, Ataxin-1, D6S504E, SCA1, Spinocerebellar ataxia type 1, ATXN1
Properties: C, C for long term storage and for short term at + 5°, If you buy Antibodies supplied by Bioss Primary Unconjugated Antibodies they should be stored frozen at - 24°
Gene target: ATXN1 (Ser775)
Short name: ATXN1 (Ser775) Antibody
Technique: antibodies against human proteins, antibodies for, Antibody
Alternative name: ATXN1 (Ser775) (Antibody to)
Alternative technique: antibodies
Identity: 10548
Gene: ATXN1 | More about : ATXN1
Long gene name: ataxin 1
Synonyms gene: SCA1
Synonyms gene name: ataxin 1) , autosomal dominant, spinocerebellar ataxia 1 (olivopontocerebellar ataxia 1
Synonyms: D6S504E ATX1
Locus: 6p22, 3
Discovery year: 1986-01-01
GenBank acession: X79204
Entrez gene record: 6310
Pubmed identfication: 1582256
RefSeq identity: NM_000332
Classification: Ataxins
Havana BLAST/BLAT: OTTHUMG00000014303
Locus Specific Databases: LRG_863

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