product summary
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company name :
MyBioSource
product type :
antibody
product name :
ARL13B Polyclonal Antibody
catalog :
MBS9126992
quantity :
0.05 mL
price :
200 USD
clonality :
polyclonal
host :
rabbit
conjugate :
nonconjugated
reactivity :
human, mouse, rat
application :
western blot
more info or order :
image
image 1 :
MyBioSource MBS9126992 image 1
Western blot analysis of extracts of SKOV3 cells, using ARL13B antibody at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (MBS128200) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 30s.
image 2 :
MyBioSource MBS9126992 image 2
Immunofluorescence analysis of C6 cells using ARL13B antibody (MBS9126992) at dilution of 1:100. Blue: DAPI for nuclear staining.
image 3 :
MyBioSource MBS9126992 image 3
Immunofluorescence analysis of U-2 OS cells using ARL13B antibody (MBS9126992) at dilution of 1:100. Blue: DAPI for nuclear staining.
product information
catalog number :
MBS9126992
products type :
Antibody
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
clonality :
Polyclonal
isotype :
IgG
host :
Rabbit
reactivity :
Human, Mouse, Rat
sequence length :
428
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 gi num :
115503786
ncbi acc num :
Q3SXY8.1
uniprot acc num :
Q3SXY8
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
size1 :
0.05 mL
price1 :
200 USD
size2 :
0.1 mL
price2 :
275
size3 :
0.2 mL
price3 :
430
more info or order :
company information
MyBioSource
P.O. Box 153308
San Diego, CA 92195-3308
sales@mybiosource.com
https://www.mybiosource.com
1-888-627-0165
headquarters: USA
MyBioSource, LLC was orginally founded in Vancouver by three enthusiastic scientists who are passionate about providing the world with the best reagents available. Together, they form a company with a big vision known as MyBioSource. MyBioSource is now located in San Diego, California, USA.

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