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RAB27A/B, Member RAS Oncogene Family (Rab27A/B) antibody

Antigen

RAB27A/B, Member RAS Oncogene Family (Rab27A/B)

Clonality Polyclonal
Host

Rabbit

Reactivity

Human

Application
Western Blotting (WB)
1 reference available
Catalog no. ABIN180234
Quantity 100 µg
Price 517.00 $   Plus shipping costs $35.00
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Availability Ships within 10 to 15 Business Days

Additional Information

Alternative name Rab27A/B
Immunogen Recombinant Rab27B protein
Isotype IgG  (Matching secondary antibodies)
Description Small GTPase Rab is a large family of membrane trafficking proteins that are conserved in all eukaryotic cells. More than 60 Rab isoforms have been reported in mice and humans, and they are believed to regulate various steps (or various types) of organelle transport. The Rab27 subfamily is phylogenetically similar to the Rab3 subfamily, and two Rab27 isoforms, Rab27A and Rab27B, are present in mice and humans. Mutations in the RAB27A gene cause human Griscelli syndrome, which is characterized by pigment dilution and immunodeficiency. The GTP-bound activated form of Rab27A regulates melanosome transport in melanocytes and secretory granule exocytosis (e.g., insulin secretion) through interaction with a specific effector molecule (e.g., Synaptotagmin-like protein (Slp) and Slac2). Rab27B is also expressed on secretory granules, the same as Rab27A, and regulates their exocytosis (e.g., amylase release from rat parotid acinar cells)
Specificity Cross-reacts with mouse and rat Rab27A/B. Does Does not crossreact with the Rab3 subfamily

Application Details

Application Notes This antibody can be used for western blotting in concentration of about 1~5g/mL.
Purification Recombinant human Rab27B
Buffer Lyophilized product from 1% BSA in PBS containing 0.05%NaN3 . Reconstitution: 1.0 ml distilled water will be added to the product, then its concentration comes to 100 ug/ml
Storage Lyophilized product, 5 years at 2 ­ 8 C : Solution, 2 years at ­20 C
Restrictions For Research Use only

Publications

Publications Kesari, Fukuda, Knoblach et al.: "Dysferlin deficiency shows compensatory induction of Rab27A/Slp2a that may contribute to inflammatory onset." in: The American journal of pathology, Vol. 173, Issue 5, pp. 1476-87, 2008 (PubMed).