DOCK8 Rabbit Polyclonal Antibody
Catalog #:EAB11174
Host / Isotype Clonality Applications MW (kDa) Reactivity
Rabbit IgG Polyclonal WB, ELISA 239 Human, Mouse
Application Key

WB-Western Blot IP-Immunoprecipitation IHC-Immunohistochemistry IHC-P-Immunohistochemistry-Paraffin
IF
-Immunofluorescence ICC-Immunocytochemistry FC-Flow Cytometry

Reactivity Key

H-Human M-Mouse R-Rat Mk-Monkey B-Bovine Pg-Pig Hm-Hamster Dg-Dog C-Chicken X-Xenopus Z-Zebrafish
Hr
-Horse All-All Species Expected

Applications Dilutions
The application notes include recommended starting dilutions;optimal dilutions/concentrations should be detemined by the end user.
WB(Westem Blotting)
IHC-P(Immunohistochemistry-Paraffin)
IF/ICC(Immunofluorescence/Immunocytochemistry)
ELISA(Enzyme-linked Immunosorbent Assay)
WB=1:500-2000
Product Information
Conjugate Unconjugate
Specificity DOCK8 Rabbit Polyclonal Antibody detects endogenous levels of DOCK8 protein.
Purification Affinity purification
Concentration 1mg/ml
Format Liquid
Formulation In PBS, pH 7.4, containing 0.02% sodium azide,0.5% BSA and 50% glycerol.
Shipping Gel Pack
Storage Store at -20°C least 1 year from the date of shipment. avoid repeated freeze/thaw cycles. Aliquots may be stored at +4°C for 1-2 weeks.
UniProt ID

Q8NF50

Entrez Gene ID

81704

Product Description

DOCK8(Dedicator of cytokinesis 8) a member of the DOCK180 family of guanine nucleotide exchange factors. DOCK8 functions as a guanine nucleotide exchange factor (GEF) that may play a role in protein activation and is thought to influence Actin organization. Defects in the gene encoding DOCK8 are associated with the pathogenesis of autosomal dominant mental retardation (MRD2), possibly due to errors in Actin-based cytoskeletal structure. Mutations in this gene also result in the autosomal recessive form of the hyper-IgE syndrome, a rare disorder characterized by immunodeficiency, recurrent infections, eczema, increased serum IgE, eosinophilia and lack of connective tissue and skeletal involvement. Multiple isoforms of DOCK8 exist due to alternative splicing events. 

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For Research Use Only, Not For Diagnostic Or Therapeutic Procedures.
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