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Specifications
- Antibody type:Primary
- Antigen name:RPGRIP1L
- Clonality:Polyclonal
- Conjugation:Alexa Fluor® 750
- Host:Rabbit
- ImmunoChemistry:Yes
- ImmunoFluorescence:Yes
- Isotype:IgG
- Western blot:Yes
- Epitope:41-140/1315
- Form:Liquid
- Antigen synonyms:Protein fantom|CORS 3|Retinitis pigmentosa GTPase regulator interacting protein 1 like|NPHP 8|NPHP8|Meckel syndrome, type 5|JBTS1|JBTS 1|Fantom|JBTS 7|MKS 5|MKS5|FTM_HUMAN|RPGRIP1-like|JBTS7|Meckel syndrome, type 1|RPGR interacting protein 1 like protein|Joubert syndrome 1|CORS3|nephrocystin 8|Joubert syndrome 7|FTM|RPGRIP1 like protein
- Modification:Unmodified
- Storage buffer:Aqueous buffered solution containing 0,01 M TBS (pH 7,4) with 1% BSA, 0,03% Proclin300 and 50% Glycerol
- Molecular weight:151 kDa
- Storage temperature:Store at −20 °C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Concentration:1 µg/µl
- Shipping temperature:4 °C
- Immunogen:KLH conjugated synthetic peptide derived from human RPGRIP1L
- Tested applications:ICC
- Purification:Purified by Protein A
- Pack type:Vial
- Pk:100 µl
Specifications
About this item
RPGRIP1L is a 1315 amino acid protein that belongs to the RPGRIP1 family and is thought to function in programmed cell death, craniofacial development and formation of the left-right axis. Existing as two alternatively spliced isoforms that localize to the cytoplasm, cytoskeleton, centrosome and cilium basal body, RPGRIP1L interacts with nephrocystin-4 and is moderately expressed in brain, retina and kidney. Containing two C2 domains, RPGRIP1L is encoded by a gene that maps to human chromosome 16q12.2. Defects in the gene encoding RPGRIP1L are the cause of Joubert syndrome type 7 (JBTS7), COACH syndrome (COACHS) and Meckel syndrome type 5 (MKS5).
Type: Primary
Antigen: RPGRIP1L
Clonality: Polyclonal
Clone:
Conjugation: ALEXA FLUOR® 750
Public Immunogen Range: 41-140/1315
Host: Rabbit
Isotype: IgG
Reactivity: