Recombinant multi-species ATXN1 protein for cell curture, in vitro study, in vivo study, benchmark, drug discovery & MOA research and positive control for the diagnosis
Genemedi produces recombinant Human, Cynomolgus/ Rhesus macaque, Rat, Mouse, Feline, Canine, Bovine, Equine ATXN1 protein for cell curture, in vitro study, in vivo study, benchmark, drug discovery & MOA research and positive control for the diagnosis.
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 40-83 CAG repeats, compared to 6-39 in the normal allele, and is associated with spinocerebellar ataxia type 1 (SCA1). Alternative splicing results in multiple transcript variants, with one variant encoding multiple distinct proteins, ATXN1 and Alt-ATXN1, due to the use of overlapping alternate reading frames. [provided by RefSeq, Nov 2017]
The Alternative Names of target: 2900016G23Rik,ATX1,ATXN1,Ataxin-1,Atx1,Atxn1,D6S504E,Gm10786,SCA1,Sca1,Spinocerebellar ataxia type 1 protein,sca1
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Product information
| Catalog No. | Product Name | Species Reactivity |
|---|---|---|
| GM-Tg-hg-IP11037-Ag-1/ GM-Tg-hg-IP11037-Ag-2 | Human ATXN1 protein | Human |
| GM-Tg-rg-IP11037-Ag-1/ GM-Tg-rg-IP11037-Ag-2 | Rat ATXN1 protein | Rat |
| GM-Tg-mg-IP11037-Ag-1/ GM-Tg-mg-IP11037-Ag-2 | Mouse ATXN1 protein | Mouse |
| GM-Tg-cynog-IP11037-Ag-1/ GM-Tg-cynog-IP11037-Ag-2 | Cynomolgus/Rhesus macaque ATXN1 protein | Cynomolgus/ Rhesus macaque |
| GM-Tg-felg-IP11037-Ag-1/ GM-Tg-felg-IP11037-Ag-2 | Feline ATXN1 protein | Feline |
| GM-Tg-cang-IP11037-Ag-1/ GM-Tg-cang-IP11037-Ag-2 | Canine ATXN1 protein | Canine |
| GM-Tg-bovg-IP11037-Ag-1/ GM-Tg-bovg-IP11037-Ag-2 | Bovine ATXN1 protein | Bovine |
| GM-Tg-equg-IP11037-Ag-1/ GM-Tg-equg-IP11037-Ag-2 | Equine ATXN1 protein | Equine |
Size: 1mg | 10mg | 100mg
Product Description
| Catalog No. |
GM-Tg-hg-IP11037-Ag-1/ GM-Tg-hg-IP11037-Ag-2;
GM-Tg-rg-IP11037-Ag-1/ GM-Tg-rg-IP11037-Ag-2;
GM-Tg-mg-IP11037-Ag-1/ GM-Tg-mg-IP11037-Ag-2; GM-Tg-cynog-IP11037-Ag-1/ GM-Tg-cynog-IP11037-Ag-2; GM-Tg-felg-IP11037-Ag-1/ GM-Tg-felg-IP11037-Ag-2; GM-Tg-cang-IP11037-Ag-1/ GM-Tg-cang-IP11037-Ag-2; GM-Tg-bovg-IP11037-Ag-1/ GM-Tg-bovg-IP11037-Ag-2; GM-Tg-equg-IP11037-Ag-1/ GM-Tg-equg-IP11037-Ag-2 |
| Products Name | ATXN1 protein |
| Species | Human, Cynomolgus/ Rhesus macaque, rat, mouse, Feline, Canine, Bovine, Equine |
| Target Name | ATXN1 |
| Protein Sub-location | Introcelluar Protein |
| Isotypes | Recombinant protein |
| Expression platform | Mammalian cell |
| Bioactivity validation | Affintiy&bioactivity validated by ELISA, cell culture validated. |
| Tag | His |
| Products description | Recombinant Human, Cynomolgus/ Rhesus macaque, Rat, Mouse, Feline, Canine, Bovine, Equine ATXN1 protein was expressed in mammalian cell expression system and is expressed with 6 HIS tag at the C-terminus for cell culture, ELISA or other affinity binding assay or functional assay development, animal model development, PK/PD model development (Pharmacokinetics & Pharmacodynamic). |
| Purity | Purity: ≥95% (SDS-PAGE) |
| Application | In vitro study, in vivo study, benchmark, positive control for the diagnosis. Biological drug disovery including cell culture, assay development, animal model development, PK/PD model development (Pharmacokinetics & Pharmacodynamic) and mechanism of action (MOA) research. |
| Formulation & Reconstitution |
Lyophilized from GM's Protein Stability Buffer2
(PSB2,Confidential Ingredients) or PBS
(pH7.4); For PSB2, reconstituted with 0.9% sodium chloride; For PBS, reconstituted with ddH2O. |
| Storage | Store at -20℃ to -80℃ under sterile conditions. Avoid repeated freeze-thaw cycles. |
Reference
About Gmab

GMab, developed by GeneMedi, constitutes an
advanced library of recombinant
monoclonal antibodies, each meticulously
designed to target specific molecular
entities. Leveraging the sophisticated
capabilities of GM’s Taurus™ and LIBRA™
platforms, GMab synthesizes antibodies
characterized by high binding affinity,
exceptional physicochemical stability, and
optimal developability profiles.
Through
expression in mammalian cell lines, GMab has
been established as a paradigmatic
reference antibody. It holds significance in
myriad domains of biological drug
discovery, encompassing cellular cultivation,
innovative assay methodologies,
strategic animal model systematization, in-depth
pharmacokinetic & pharmacodynamic
(PK/PD) modeling, and intricate mechanism of
action (MOA) investigations.