Name : ATXN3L Antibody
Supplier : BIOSS PRIMARY UNCONJUGATED ANTIBODIES
Price :263
SKU : GEN5872626789
| Long name | ATXN3L Primary Polyclonal Antibody |
| Also known as | ATXN3L PAb |
| Category | Primary Antibodies |
| Conjugation | Unconjugated |
| Target Antigen | ATXN3L |
| Specificity | This is a highly specific antibody against ATXN3L |
| Modification(s) | None |
| Modification site(s) | Unmodified antibody |
| Clonality | Polyclonal antibody |
| Clone number | Polyclonal antibody |
| Concentration | 1ug per 1ul |
| Source | This antibody was obtained by immunization of the host with KLH conjugated synthetic peptide derived from human ATXN3L |
| Gene ID number | 92552 |
| 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 | 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 | Longer expansions result in earlier onset and more severe clinical manifestations of the disease, Patients show progressive incoordination of gait and often poor coordination of hands, SCA3 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders, The molecular defect in SCA3 is the a CAG repeat expansion in ATXN3 coding region, also known as Machado-Joseph disease (MJD), bulbar and extrapyramidal signs, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord, ophthalmoplegia, peripheral neuropathy and dementia, speech and eye movements, Defects in ATXN3 are the cause of spinocerebellar ataxia type 3 (SCA3) |
| 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 | ATXN3L, MJDL, Machado-Joseph disease protein 1-like, Putative ataxin-3-like protein, ATX3L_HUMAN |
| 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 | ATXN3L |
| Short name | ATXN3L Antibody |
| Technique | antibodies against human proteins, antibodies for, Antibody |
| Alternative name | ATXN3L (Antibody to) |
| Alternative technique | antibodies |
| Identity | 24173 |
| Gene | ATXN3L |
| Long gene name | ataxin 3 like |
| Synonyms gene name | ataxin 3-like |
| Synonyms | MJDL |
| Locus | Xp22, 2 |
| Discovery year | 2004-08-20 |
| Entrez gene record | 92552 |
| RefSeq identity | NM_001135995 |
| Classification | MJD deubiquinating enzymes |
| Havana BLAST/BLAT | OTTHUMG00000021146 |
| Locus Specific Databases | Mental Retardation database |