Name : SPG3A/Atlastin Antibody
Supplier : BIOSS PRIMARY UNCONJUGATED ANTIBODIES
Price :263
SKU : GEN3941752475
| Long name | SPG3A/Atlastin Primary Polyclonal Antibody |
| Also known as | SPG3A/Atlastin PAb |
| Category | Primary Antibodies |
| Conjugation | Unconjugated |
| Target Antigen | SPG3A/Atlastin |
| Specificity | This is a highly specific antibody against SPG3A/Atlastin |
| 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 SPG3A/Atlastin |
| 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 | HSP primarily affects long corticospinal neurons and causes spastic lower extremity weakness, Hereditary spastic paraplegia (HSP) is an inherited neurodegenerative disorder that is characterized by retrograde axonal degeneration, Mutations in the Atlastin gene (SPG3A) account for approximately 10% of all autosomal dominant HSPs, Spastin, The Atlastin proteins, This Spastin/Atlastin binding may be involved in the biochemical pathway that leads to HSP development, a microtubule (MT)-severing AAA ATPase, also designated SPG3A and guanylate-binding protein 3, comprise a Dynamin superfamily that plays a role in axonal maintenance, integral membrane proteins that function as GTPases, is a binding partner of Atlastin that is involved in membrane dynamics, while mutations in the Spastin gene (SPG4) account for almost 40%, Atlastins are Golgi-localized |
| 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 | ATLA1_HUMAN, Atlastin GTPase 1, Atlastin-1, Atlastin1, Brain specic GTP binding protein, Brain-specic GTP-binding protein, FSP1, GBP-3, GBP3, GTP-binding protein 3, Guanine nucleotide-binding protein 3, Guanylate binding protein 3, HSN1D, SPG 3A, SPG3, SPG3A, Spastic paraplegia 3 protein A, atl1, hGBP3, AD FSP |
| 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 | SPG3A/Atlastin |
| Short name | SPG3A/Atlastin Antibody |
| Technique | antibodies against human proteins, antibodies for, Antibody |
| Alternative name | SPG3A/Atlastin (Antibody to) |
| Alternative technique | antibodies |
| Identity | 11231 |
| Gene | ATL1 |
| Long gene name | atlastin GTPase 1 |
| Synonyms gene | SPG3 SPG3A |
| Synonyms gene name | spastic paraplegia 3A (autosomal dominant) |
| Synonyms | FSP1 AD-FSP |
| Synonyms name | atlastin |
| Locus | 14q22, 1 |
| Discovery year | 1993-10-28 |
| GenBank acession | AF131801 |
| Entrez gene record | 51062 |
| Pubmed identfication | 8252041 7825576 |
| Havana BLAST/BLAT | OTTHUMG00000140297 |
| Locus Specific Databases | LRG_360 |