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AGC1 antibody

SEQer™ Antibodies - Successful results in complex assays

  • Bioinformatic design which selects the optimal 100 amino acid residues for high specificity with low cross reactivity
  • In-vivo expressed antigen which recognize protein's native conformation with multiple epitopes
  • Excellent tools for immuno-precipitation, sandwich ELISA, antibody array, IF, immunohistochemistry, and more

SDIX's antibodies are exclusively distributed by Novus Biologicals.   Click the Purchase section below and "Add to Cart" below to be taken to Novus Biological's web site to complete your order.   Or call Novus Biologicals toll-free (888)506-6887, 9am-7:30pm EST.  

Description 

Reactivity: Human
Source: Rabbit Polyclonal
Immunogen: In vivo generated recombinant protein fragment
Purification: Affinity purified using a recombinant protein fragment
QC Test: QC tested by ELISA using a recombinant protein
Buffer: 20 mM Potassium Phosphate, 150 mM Sodium Chloride, pH 7.0
Synonyms: Aggrecan core protein antibody, AGC1 antibody, Aggrecan 1 antibody, Aggrecan structural proteoglycan of cartilage antibody, Cartilage specific proteoglycan core protein antibody, CSPCP antibody, Chondroitin sulfate proteoglycan core protein 1 antibody, CSPG1 antibody, JSCATE antibody, MSK 16 antibody, SEDK antibody.
Type: SeqAntibodies Icon
Datasheet:

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Catolog # Size Price  
3533.00.02 50 ug Click for Price Add to Cart

Background Data 

GeneFunction: This proteoglycan is a major component of extracellular matrix of cartilagenous tissues. A major function of this protein is to resist compression in cartilage. It binds avidly to hyaluronic acid via an N-terminal globular region.
BelongsTo:
TissueLoc: Restricted to cartilages.
SubCellLoc: Secreted, extracellular space, extracellular matrix (By similarity).
DiseaseAssoc: Defects in AGC1 are the cause of spondyloepiphyseal dysplasia type Kimberley (SEDK) [MIM:608361]. Spondyloepiphyseal dysplasias are a heterogeneous group of congenital chondrodysplasias that specifically affect epiphyses and vertebrae. The autosomal dominant SEDK is associated with premature degenerative arthropathy.
Pathway:
Topology: Nonmembrane Protein