ARL13B Monoclonal antibody, PBS Only

ARL13B Monoclonal Antibody for WB, IF/ICC, IF-Fro, Indirect ELISA

Host / Isotype

Mouse / IgG2a

Reactivity

human, mouse, pig, canine

Applications

WB, IF/ICC, IF-Fro, Indirect ELISA

Conjugate

Unconjugated

CloneNo.

1H6C3

Cat no : 66739-1-PBS

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Synonyms

ARL2-like protein 1, ARL2L1, ARL2 like protein 1, ADP-ribosylation factor-like protein 2-like 1, ADP-ribosylation factor-like protein 13B



产品信息

66739-1-PBS targets ARL13B in WB, IF/ICC, IF-Fro, Indirect ELISA applications and shows reactivity with human, mouse, pig, canine samples.

Tested Applications WB, IF/ICC, IF-Fro, Indirect ELISA Application Description
Tested Reactivity human, mouse, pig, canine
Immunogen ARL13B fusion protein Ag12031 种属同源性预测
Host / Isotype Mouse / IgG2a
Class Monoclonal
Type Antibody
Full Name ADP-ribosylation factor-like 13B
Synonyms ARL2-like protein 1, ARL2L1, ARL2 like protein 1, ADP-ribosylation factor-like protein 2-like 1, ADP-ribosylation factor-like protein 13B
Calculated Molecular Weight 48 kDa
Observed Molecular Weight 60 kDa
GenBank Accession NumberBC094725
Gene Symbol ARL13B
Gene ID (NCBI) 200894
RRIDAB_2882088
Conjugate Unconjugated
Form Liquid
Purification MethodProtein A purification
UNIPROT IDQ3SXY8
Storage Buffer PBS Only
Storage ConditionsStore at -80°C.
The product is shipped with ice packs. Upon receipt, store it immediately at -80°C

背景介绍

ARL13B, also named as ARL2L1, is a small ciliary G protein of the Ras superfamily. Localized in the cilia, it is required for cilium biogenesis and sonic hedgehog signaling. Defects in ARL13B are the cause of Joubert syndrome (JS) which is an autosomal recessive disorder characterized by a distinctive cerebellar malformation (PMID: 19906870). Arl13b is predicted to be a 48 kDa protein, and the 60 kDa band is likely to represent a modified form of Arl13b. ARL13B can be used to mark the cilia (PMID:22072986).