catalog number :
MBS9126992
products full name :
ARL13B Polyclonal Antibody
products short name :
[ARL13B]
products name syn :
[ARL13B; ARL2L1; JBTS8; ADP ribosylation factor like GTPase 13B]
other names :
[ADP-ribosylation factor-like protein 13B; ADP-ribosylation factor-like protein 13B; ADP-ribosylation factor-like protein 13B; ARL2-like protein 1; ADP-ribosylation factor-like 2-like 1; ADP-ribosylation factor-like 13B; ADP-ribosylation factor-like protein 2-like 1; ARL2-like protein 1]
products gene name :
[ARL13B]
other gene names :
[ARL13B; ARL13B; JBTS8; ARL2L1; ARL2L1; ARL2-like protein 1]
uniprot entry name :
AR13B_HUMAN
reactivity :
Human, Mouse, Rat
purity :
Affinity Purification
form :
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
storage stability :
Store at -20°C. Avoid freeze / thaw cycles.
tested application :
Western Blot (WB)
app notes :
Recommended Dilutions: WB 1:500 - 1:2000
image1 heading :
Western Blot (WB)
image2 heading :
Immunofluorescence (IF)
image3 heading :
Immunofluorescence (IF)
image4 heading :
Immunofluorescence (IF)
image4 description :
Immunofluorescence analysis of L929 cells using ARL13B antibody (MBS9126992) at dilution of 1:100. Blue: DAPI for nuclear staining.
other info1 :
Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-240 of human ARL13B (NP_878899.1).
products categories :
Polyclonal
products description :
This gene encodes a member of the ADP-ribosylation factor-like family. The encoded protein is a small GTPase that contains both N-terminal and C-terminal guanine nucleotide-binding motifs. This protein is localized in the cilia and plays a role in cilia formation and in maintenance of cilia. Mutations in this gene are the cause of Joubert syndrome 8. Alternate splicing results in multiple transcript variants.
ncbi mol weight :
Observed: 49kDa. Calculated: 36kDa/37kDa/48kDa
ncbi pathways :
ARL13B-mediated Ciliary Trafficking Of INPP5E Pathway (1127508); Assembly Of The Primary Cilium Pathway (1127502); Cargo Trafficking To The Periciliary Membrane Pathway (1127504); Organelle Biogenesis And Maintenance Pathway (1127494)
ncbi summary :
This gene encodes a member of the ADP-ribosylation factor-like family. The encoded protein is a small GTPase that contains both N-terminal and C-terminal guanine nucleotide-binding motifs. This protein is localized in the cilia and plays a role in cilia formation and in maintenance of cilia. Mutations in this gene are the cause of Joubert syndrome 8. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]
uniprot summary :
ARL13B: Defects in ARL13B are the cause of Joubert syndrome type 8 (JBTS8). JBTS is an autosomal recessive disorder presenting with cerebellar ataxia, oculomotor apraxia, hypotonia, neonatal breathing abnormalities and psychomotor delay. Neuroradiologically, it is characterized by cerebellar vermis hypoplasia/aplasia, thickened and reoriented superior cerebellar peduncles, and an abnormally large interpeduncular fossa, giving the appearance of a molar tooth on transaxial slices (molar tooth sign). Additional variable features include retinal dystrophy and renal disease. Belongs to the small GTPase superfamily. Arf family. 2 isoforms of the human protein are produced by alternative splicing. Protein type: G protein, monomeric; G protein, monomeric, ARF. Chromosomal Location of Human Ortholog: 3q11.1. Cellular Component: intracellular; cilium. Molecular Function: protein binding; GTP binding. Biological Process: formation of radial glial scaffolds; smoothened signaling pathway; dorsal/ventral pattern formation; interneuron migration from the subpallium to the cortex; sensory cilium biogenesis; organelle organization and biogenesis; small GTPase mediated signal transduction; neural tube patterning; cilium biogenesis; heart looping. Disease: Joubert Syndrome 8