C1QA Mouse Monoclonal Antibody [Clone ID: JL-1]

CAT#: AM26376BT-N

C1QA mouse monoclonal antibody, clone JL-1, Biotin

Specifications

Product Data

• Clone Name: JL-1
• Applications: ELISA, FN, IF, IHC, WB
• Recommended Dilution: Immunohistochemistry on Frozen Sections (Ref.1): Stains tissue sections which were fixed in acetone. As positive control a polyclonal anti-C1q antibody was used and as negative control an isotype matched monoclonal antibody (Ref.1). The typical starting working dilution is 1/50.
  Functional assays (Ref.1): Antibody JL-1 was administered to mice resulting in depletion of circulating C1q, glomerular deposition of C1q and induction of anti-C1q autoantibodies in susceptible mice. As a negative control an isotype matched monoclonal antibody was used (Ref.1).
  Immunoassays (Ref.1,2).
  Immunofluorescence (Ref.1).
  Western blot (Ref.3): The typical starting working dilution is 1/50.
  Positive Control: Spleen and kidney tissue of wild-type mice (Ref.1).
  Negative Control: Spleen and kidney tissue of C1q -/- mice (Ref.1).
• Reactivities: Human, Mouse, Rat
• Host: Mouse
• Isotype: IgG2b
• Clonality: Monoclonal
• Immunogen: Purified mouse C1q
• Specificity:
  The monoclonal antibody JL-1 recognizes the collagen-like region (CLR) of mouse C1q.
• Formulation: PBS
  Label: Biotin
  State: Liquid 0.2 µm filtered Ig fraction
  Stabilizer: 0.1% BSA
  Preservative: 0.02% Sodium Azide
• Concentration: lot specific
• Purification: Protein G Chromatography
• Conjugation: Biotin
• Storage: Store undiluted at 2-8°C.
  DO NOT FREEZE!
  
• Stability: Shelf life: one year from despatch.
• Gene Name: complement component 1, q subcomponent, A chain
• Database Link:
  Entrez Gene 712 Human
  UniProt ID P02745
• Background:

  C1q is a 459 kDa molecule consisting of three individual polypeptide chains. The antibody has been generated by immunization of C1q-/- C57BL/6 mice with purified mouse C1q.
  C1q forms together with C1r and C1s the C1 macromolecule, the first component of the classical complement pathway. Interaction of immune complexes with C1q induces a conformational change within the C1 complex, which results in activation of the classical pathway. C1q functions as recognition unit by binding to the heavy chain of IgG or IgM (Fc gamma and Fc micro) provided that the immunoglobulins are bound to their antigen. Furthermore, C1q can also recognize molecular patterns associated with pathogens and it can bind to apoptotic blebs, where it activates the classical complement pathway and mediates phagocytosis. As such, C1q promotes the clearance of apoptotic cells and subsequent exposure of auto antigens, thereby preventing stimulation of the immune system.
  C1q is predominantly produced by macrophages but also by follicular dendritic cells, interdigitating cells and cells of the monocyte-macrophage lineage. C1q deficiency has a profound effect on host defence and clearance of immune complexes. Absence of C1q may cause autoimmunity by impairment of the clearance of apoptotic cells. Inherited C1q deficiency is also associated with the development of systemic lupus erythematosus (SLE).

• Synonyms: Complement C1q, Complement 1q