Goat Anti-Asporin / ASPN Antibody

This goat IgG polyclonal antibody was generated against peptide sequence C-IHENKVKKIQKD from the internal region of asporin (ASPN) and recognizes human, mouse, and rat ASPN.

Highlights:

  • Reacts with human, mouse, and rat ASPN
  • Suitable for Peptide ELISA, Western Blot, and Immunofluorescence applications
  • Polymorphisms are associated with osteoarthritis and intervertebral disc disease

Asporin (ASPN) is an extracellular matrix protein that is a member of the small leucine-rich proteoglycan family of proteins. ASPN is present in bone, cartilage, and the periodontal ligament. ASPN has a unique aspartic acid repeat at the N terminus of the mature protein. Polymorphisms in the aspartic acid repeat region of the gene are associated with osteoarthritis and intervertebral disc disease.

Catalog Number Product DataSheet Size AVAILABILITY Price Qty
EB06670
Goat Anti-Asporin / ASPN Antibody
100ug specific antibody in 200ul In stock
Regular Price:$415.00
On Sale:
Specifications

Product Type: Antibody
Name: Goat Anti-Asporin / ASPN Antibody
Alternative Name(s): Periodontal ligament-associated protein 1, PLAP-1, SLRR1C
Accession ID: NP_060150.4
Antigen: Asporin / ASPN
Isotype: IgG
Clonality: Polyclonal
Reactivity: Human, Mouse, Rat
Specificity: Asporin / ASPN
Immunogen: CIHENKVKKIQKDT
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

(0.1µg/ml) staining of Human Tonsil (A), (0.3ug/ml) Human Uterus (B), Mouse Skeletal Muscle (C) (1ug/ml) Rat Skeletal Muscle (D) and negative control Human Cerebellum (E) lysate (35µg protein in RIPA buffer).Detected by chemiluminescence.

Immunofluorescence

WB Data

Immunofluorescence analysis of paraformaldehyde fixed HeLa cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10ug/ml) followed by Alexa Fluor 488 secondary antibody (4ug/ml), showing nuclear membrane staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10ug/ml) followed by Alexa Fluor 488 secondary antibody (4ug/ml).

References

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