RPGRIP1L polyclonal antibody
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More Files
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Western Blot (Tissue lysate)
RPGRIP1L polyclonal antibody (Cat # PAB7600) (0.3 ug/mL) staining of human brain (cerebellum) lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
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Specification
Product Description
Goat polyclonal antibody raised against synthetic peptide of RPGRIP1L.
Immunogen
A synthetic peptide corresponding to human RPGRIP1L.
Sequence
C-DKENNKAKRDILK
Host
Goat
Theoretical MW (kDa)
151
Reactivity
Human
Form
Liquid
Purification
Antigen affinity purification
Concentration
0.5 mg/mL
Quality Control Testing
Antibody Reactive Against Synthetic Peptide.
Recommend Usage
ELISA (1:64000)
Western Blot (0.3-1 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
Storage Instruction
Store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot (Tissue lysate)
RPGRIP1L polyclonal antibody (Cat # PAB7600) (0.3 ug/mL) staining of human brain (cerebellum) lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.Enzyme-linked Immunoabsorbent Assay
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Gene Info — RPGRIP1L
Entrez GeneID
23322Protein Accession#
NP_056087.2Gene Name
RPGRIP1L
Gene Alias
CORS3, DKFZp686C0668, JBTS7, KIAA1005, MKS5, NPHP8
Gene Description
RPGRIP1-like
Omim ID
610937Gene Ontology
HyperlinkGene Summary
The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq
Other Designations
RPGR-interacting protein 1-like protein|protein fantom
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Interactome
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Disease
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Publication Reference
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Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome.
Arts HH, Doherty D, van Beersum SE, Parisi MA, Letteboer SJ, Gorden NT, Peters TA, Marker T, Voesenek K, Kartono A, Ozyurek H, Farin FM, Kroes HY, Wolfrum U, Brunner HG, Cremers FP, Glass IA, Knoers NV, Roepman R.
Nature Genetics 2007 Jul; 39(7):882.
Application：IEM, IF, Human, Rat, ARPE-19 cells, Rat retina.
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Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome.
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