Name : Doppel/DPL Antibody
Supplier : BIOSS PRIMARY UNCONJUGATED ANTIBODIES
Price :263
SKU : GEN5279044460
| Long name | Doppel/DPL Primary Polyclonal Antibody |
| Also known as | Doppel/DPL PAb |
| Category | Primary Antibodies |
| Conjugation | Unconjugated |
| Target Antigen | Doppel/DPL |
| Specificity | This is a highly specific antibody against Doppel/DPL |
| 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 Doppel |
| 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 | BSE in cattle, Dpl does not appear to contribute to prion disease progression, Dpl is also thought to play a role in angiogenesis, Dpl is characterized by an alpha-helical conformation, Dpl is highly expressed in adult testis and heart and is detectable in the brain of neonatal mice, Infectious PrPSc is highly expressed in the brain of animals affected by TSEs, The PRND gene locus, and Cruetzfeldt-Jacob disease in humans, and it is presented on the cell surface by a glycosylphosphatidylinositol anchor, and two N-linked oligosaccharides, but ectopic expression of Dpl is implicated in neuronal degeneration of ataxic PRP-deficient mice, encodes for the doppel protein (Dpl), including scrapie in sheep, infectious or sporadic, intramolecular disulfide bonds, lethal neurodegenerative disorders involving alterations of the prion protein (PrP), located on human chromosome 20p, specifically maturation of the blood-brain barrier, which exhibits approximately 25% sequence homology with PrP, Prion diseases or transmissible spongiform encephalopathies (TSEs) are manifested as genetic |
| 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 | Dublet, MGC41841, PRND, PRND_HUMAN, PrPLP, Prion gene complex downstream, Prion like protein doppel, Prion protein 2, Prion protein 2 dublet, Prion-like protein doppel, DPL |
| 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 | Doppel/DPL |
| Short name | Doppel/DPL Antibody |
| Technique | antibodies against human proteins, antibodies for, Antibody |
| Alternative name | Doppel/DPL (Antibody to) |
| Alternative technique | antibodies |
| Identity | 15748 |
| Gene | PRND |
| Long gene name | prion like protein doppel |
| Synonyms gene name | prion protein 2 (dublet) |
| Synonyms | DPL dJ1068H6, 4 DOPPEL PrPLP |
| Synonyms name | prion-like protein doppel downstream prion protein-like gene |
| Locus | 20p13 |
| Discovery year | 2001-05-30 |
| GenBank acession | AF106918 |
| Entrez gene record | 23627 |
| Pubmed identfication | 10525406 10577243 |
| RefSeq identity | NM_012409 |
| Havana BLAST/BLAT | OTTHUMG00000031789 |