ARG55740

anti-RAB27A antibody

anti-RAB27A antibody for ICC/IF,IHC-Frozen sections,IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human,Mouse,Rat,Dog,Monkey

Overview

Product Description Goat Polyclonal antibody recognizes RAB27A
Tested Reactivity Hu, Ms, Rat, Dog, Mk
Tested Application ICC/IF, IHC-Fr, IHC-P, WB
Specificity Detects Rab27a by Western blot in the following human, rat and mouse whole cell lysates and transfected cells with GFP-Rab27a.
Host Goat
Clonality Polyclonal
Isotype IgG
Target Name RAB27A
Antigen Species Mouse
Immunogen Purified recombinant peptide around aa. 120 (C-terminus) of Mouse Rab27a 
Conjugation Un-conjugated
Alternate Names ash; Ras-related protein Rab-27A

Application Instructions

Application Suggestion
Tested Application Dilution
ICC/IF1:50-1:200
IHC-Fr1:50-1:200
IHC-P1:50-1:200
WB1:250-1:1000
Application Note IHC-P: Antigen retrieval: Heat-induced.
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Affinity purification with immunogen.
Buffer PBS, 0.05% Sodium azide and 20% Glycerol
Preservative 0.05% Sodium azide
Stabilizer 20% Glycerol
Concentration 1 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. 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: 11891 Mouse RAB27A

GeneID: 50645 Rat RAB27A

GeneID: 5873 Human RAB27A

Gene Symbol Rab27a
Gene Full Name RAB27A, member RAS oncogene family
Background The protein encoded by this gene is a member of the Rab family of proteins, which is the largest family within the Ras superfamily of GTPases. This gene product is thought to regulate vesicular transport, together with its specific effectors. Mutations in this gene cause several defects, including actin-based melanosome transport defects and immunodeficiency. Mutations in the human ortholog of this gene are associated with Griscelli syndrome type 2. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]
Function Plays a role in cytotoxic granule exocytosis in lymphocytes. Required for both granule maturation and granule docking and priming at the immunologic synapse (By similarity). [UniProt]
Calculated MW 25 kDa