Name : RPGRIP1L Antibody
Supplier : BIOSS PRIMARY UNCONJUGATED ANTIBODIES
Price :263
SKU : GEN5399094414
| Long name | RPGRIP1L Primary Polyclonal Antibody |
| Also known as | RPGRIP1L PAb |
| Category | Primary Antibodies |
| Conjugation | Unconjugated |
| Target Antigen | RPGRIP1L |
| Specificity | This is a highly specific antibody against RPGRIP1L |
| 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 RPGRIP1L |
| 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 | COACH syndrome (COACHS) and Meckel syndrome type 5 (MKS5), Containing two C2 domains, Defects in the gene encoding RPGRIP1L are the cause of Joubert syndrome type 7 (JBTS7), Existing as two alternatively spliced isoforms that localize to the cytoplasm, RPGRIP1L interacts with nephrocystin-4 and is moderately expressed in brain, RPGRIP1L is encoded by a gene that maps to human chromosome 16q12, centrosome and cilium basal body, craniofacial development and formation of the left-right axis, cytoskeleton, retina and kidney, 2, 315 amino acid protein that belongs to the RPGRIP1 family and is thought to function in programmed cell death, RPGRIP1L is a 1 |
| 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 | CORS3, FTM, FTM_HUMAN, Fantom, JBTS 1, JBTS 7, JBTS1, JBTS7, Joubert syndrome 1, Joubert syndrome 7, MKS 5, MKS5, Meckel syndrome, Meckel syndrome, NPHP 8, NPHP8, Protein fantom, RPGR interacting protein 1 like protein, RPGRIP1 like protein, RPGRIP1-like, Retinitis pigmentosa GTPase regulator interacting protein 1 like, nephrocystin 8, type 1, type 5, CORS 3 |
| 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 | RPGRIP1L |
| Short name | RPGRIP1L Antibody |
| Technique | antibodies against human proteins, antibodies for, Antibody |
| Alternative name | RPGRIP1L (Antibody to) |
| Alternative technique | antibodies |
| Identity | 29168 |
| Gene | RPGRIP1L |
| Long gene name | RPGRIP1 like |
| Synonyms gene name | RPGRIP1-like |
| Synonyms | KIAA1005 CORS3 JBTS7 MKS5 NPHP8 FTM PPP1R134 |
| Synonyms name | fantom homolog Meckel syndrome, regulatory subunit 134 , type 5 protein phosphatase 1 |
| Locus | 16q12, 2 |
| Discovery year | 2007-05-14 |
| Entrez gene record | 23322 |
| Pubmed identfication | 10231032 |
| RefSeq identity | NM_015272 |
| Classification | Protein phosphatase 1 regulatory subunits C2 domain containing |
| Havana BLAST/BLAT | OTTHUMG00000173125 |
| Locus Specific Databases | LRG_696 |