Goat Anti-EEA1 (aa821-835) Antibody

This goat IgG polyclonal antibody was generated against peptide sequence CQETKIQHEELNNRIQ from the Internal Region of early endosome antigen 1 (EEA1) and recognizes human and mouse EEA1.

Highlights:

  • Reacts with human and mouse EEA1
  • Suitable for Peptide ELISA, Western Blot, and Immunofluorescence applications
  • Associated with Subacute Cutaneous Lupus Erythematosus and Cutaneous Lupus Erythematosus

Early endosomes are involved in receiving endocytosed materials and sorting them for transport to late endosomes or recycling them to the plasma membrane. Early endosome antigen 1 (EEA1) is associated with early endosomes and is involved in endosome trafficking by binding phospholipid vesicles containing phosphatidylinositol 3-phosphate. Diseases associated with EEA1 include Subacute Cutaneous Lupus Erythematosus and Cutaneous Lupus Erythematosus.

Catalog Number Product DataSheet Size AVAILABILITY Price Qty
EB11689
Goat Anti-EEA1 (aa821-835) Antibody
100ug specific antibody in 200ul In stock
Regular Price:$415.00
On Sale:
Specifications

Product Type: Antibody
Name: Goat Anti-EEA1 (aa821-835) Antibody
Alternative Name(s): Endosome-associated protein p162, Zinc finger FYVE domain-containing protein 2, ZFYVE2
Accession ID: NP_003557.2
Antigen: EEA1 (aa821-835)
Isotype: IgG
Clonality: Polyclonal
Reactivity: Human, Mouse
Specificity: EEA1 (aa821-835)
Immunogen: CQETKIQHEELNNRIQ
Species Immunized: Goat
Epitope: Internal Region
Purification Method: Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide
Buffer: Supplied at 0.5 mg/ml in Tris saline, 0.02% sodium azide, pH7.3 with 0.5% bovine serum albumin.
Tested Applications: Pep-ELISA, WB, IF
Storage: Aliquot and store at -20C. Minimize freezing and thawing.
Shipped: Cold Packs

Documentation
Data

Western Blot

WB Data

(0.3µg/ml) staining of HEK293 lysate (35µg protein in RIPA buffer). Detected by chemiluminescence.

Immunofluorescence

WB Data

Immunofluorescence analysis of paraformaldehyde fixed NIH3T3 cells, permeabilized with 0.15% Triton. Primary incubation 1hr (5ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing vesicle/cytoplasmic staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (5ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml).

References

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