ATXN1 (Ser775) Antibody, Cy5 Conjugated

Catalog number:	bs-3008R-Cy5 Buy Now
Price:	453 €
Supplier:	MBS Polyclonals
Product name:	ATXN1 (Ser775) Antibody, Cy5 Conjugated
Quantity:	100ug
Related search:	antibody gene antibodies sca ataxia synonyms allele

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Long name:	Cy5 Conjugated, ATXN1 (Ser775) Polyclonal Antibody
Category:	Conjugated Primary Antibodies
Conjugation:	5, Cy5
Host Organism:	Rabbit (Oryctolagus cuniculus)
Target Antigen:	ATXN1 Ser775
Specificity:	This is a highly specific antibody against ATXN1 Ser775
Modification:	Phosphorylation
Modification site:	Ser775
Clonality:	Polyclonal
Clone:	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)
Recommended dilutions:	IF(IHC-P)(1:50-200)
Crossreactivity:	Mouse, Rat, Human
Crossreactive species details:	not every possible cross-reactivity is known, Due to limited amount of testing and knowledge
Antigen background:	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 refrigerated at 2 to 8 degrees Celcius for up to 1 year, 09% sodium azide, Keep the antibody in an aqueous buffered solution containing 1% BSA
Excitation Emission:	625, 650nm/670nm
Synonyms:	D6S504E ATX1
Properties:	Cy5 antibodies are excited by the 650-nanometer wave of an argon laser and detected at a 670-nanometer captor, C, C for long term storage and for short term at + 5°, If you buy Antibodies supplied by Bioss Primary Conjugated Antibodies they should be stored frozen at - 24°
Gene target:	ATXN1 (Ser775) Conjugated
Short name:	Conjugated, ATXN1 (Ser775) Antibody
Technique:	antibodies against human proteins, antibodies for, antibody Conjugates, Antibody
Label:	Cy5
Alternative name:	cyanine 5 coupled, 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
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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