ARG45241

anti-ARL13B antibody

anti-ARL13B antibody for Flow cytometry,ICC/IF,IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human,Mouse,Rat

Overview

Product Description Polyclonal antibody recognizes ARL13B
Tested Reactivity Hu, Ms, Rat
Tested Application FACS, ICC/IF, IHC-P, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name ARL13B
Antigen Species Human
Immunogen Recombinant protein containing to human ARL13B.
Conjugation Un-conjugated
Alternate Names ARL13B; ARF Like GTPase 13B; ADP Ribosylation Factor Like GTPase 13B; ARL2L1; JBTS8; ADP-Ribosylation Factor-Like Protein 13B; ADP-Ribosylation Factor-Like 2-Like 1; ARL2-Like Protein 1; DKFZp761H079; ADP-Ribosylation Factor-Like Protein 2-Like 1; ADP-Ribosylation Factor Like GTPase 13B; ADP-Ribosylation Factor-Like 13B

Application Instructions

Application Suggestion
Tested Application Dilution
FACS1 - 3 µg/10^6 cells
ICC/IF5 μg/ml
IHC-P2-5 μg/ml
WB0.25-0.5 μg/ml
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Observed Size 55 kDa

Properties

Form Liquid
Purification Affinity purification with immunogen.
Buffer 0.2% Na2HPO4, 0.9% NaCl and 4% Trehalose.
Stabilizer 4% Trehalose
Concentration 0.5 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 200894 Human ARL13B

GeneID: 68146 Mouse ARL13B

Swiss-port # Q3SXY8 Human ADP-ribosylation factor-like protein 13B

Swiss-port # Q640N2 Mouse ADP-ribosylation factor-like protein 13B

Gene Symbol ARL13B
Gene Full Name ARF Like GTPase 13B
Background 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]
Function Cilium-specific protein required to control the microtubule-based, ciliary axoneme structure. May act by maintaining the association between IFT subcomplexes A and B. Binds GTP but is not able to hydrolyze fit; the GTPase activity remains unclear. Required to pattern the neural tube. Involved in cerebral cortex development: required for the initial formation of a polarized radial glial scaffold, the first step in the construction of the cerebral cortex, by regulating ciliary signaling. Regulates the migration and placement of postmitotic interneurons in the developing cerebral cortex. Plays a role in ciliar trafficking of phosphatidylinositol phosphatase INPP5E in ciliogenesis. [UniProt]
Cellular Localization Cell membrane ; Cell projection ; Cilium ; Cytoplasm ; Cytoskeleton ; Membrane. [UniProt]
Calculated MW 49 kDa
PTM Isopeptide bond ; Lipoprotein ; Palmitate ; Ubl conjugation. [UniProt]