| Catalog number: | bs-11025R |
|---|---|
| Price: | 729 € |
| Supplier: | genways |
| Product name: | Gigaxonin Antibody |
| Quantity: | 1 tube |
| Related search: |
| Long name: | Gigaxonin Primary Polyclonal Antibody |
|---|---|
| Also known as: | Gigaxonin PAb |
| Category: | Primary Antibodies |
| Conjugation: | Unconjugated |
| Target Antigen: | Gigaxonin |
| Specificity: | This is a highly specific antibody against Gigaxonin |
| 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 Gigaxonin |
| Tested Applications: | IF(IHC-P), IHC-P |
| Recommended dilutions: | IF(IHC-P)(1:50-200), IHC-P(1:100-500) |
| 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: | GAN1, Gigaxonin is a member of the cytoskeletal BTB/kelch repeat family and influences cytoskeletal organization and dynamics, Mutations in the Gigaxonin gene result in human giant axonal neuropathy (GAN), Overexpression of MAP1B may lead to neuronal cell death, The amino terminal BTB domain of gigaxonin binds to the ubiquitin-activating enzyme E1, also refered to as giant axonal neuropathy, an autosomal recessive neurodegenerative disorder characterized by axonal degeneration caused by cytoskeletal abnormalities, and tags it for degredation, controls protein degradation and is essential for neuronal function and survival, including accumulated intermediate filaments, or KLHL16, playing a large role in neurofilament architecture, whereas a reduction of MAP1B significantly improves the survival rate of neurons, while the carboxy-terminal kelch repeat domain interacts directly with the light chain of microtubule-associated protein 1B (MAP1B), Gigaxonin |
| 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: | GAN, GAN1, GAN_HUMAN, KLHL16, Kelch-like protein 16, giant axonal neuropathy, FLJ38059 |
| 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: | Gigaxonin |
| Short name: | Gigaxonin Antibody |
| Technique: | antibodies against human proteins, antibodies for, Antibody |
| Alternative name: | Gigaxonin (Antibody to) |
| Alternative technique: | antibodies |
| Identity: | 4137 |
| Gene: | GAN | More about : GAN |
| Long gene name: | gigaxonin |
| Synonyms gene name: | giant axonal neuropathy (gigaxonin) |
| Synonyms: | GAN1 KLHL16 |
| Synonyms name: | kelch-like family member 16 |
| Locus: | 16q23, 2 |
| Discovery year: | 1998-09-14 |
| GenBank acession: | AF291673 |
| Entrez gene record: | 8139 |
| Pubmed identfication: | 9450783 11062483 |
| Classification: | BTB domain containing Kelch like |
| Havana BLAST/BLAT: | OTTHUMG00000137627 |
| Locus Specific Databases: | Inherited Peripheral Neuropathies Mutation Database LRG_242 |
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