产品介绍
Quidel Polyclonal Antiserum to Human C3 Protein
A304
2.0 mL
Whole Antiserum
≤ 0.1% Sodium Azide
Baboon, Horse, Hamster, Rabbit, Guinea Pig, Rat, Mouse, Rhesus macaque
2°C to 8°C (≤ 30 days)
For long-term storage (> 30 days), aliquot and store at ≤ –20°C. Avoid repeated freeze-thaw.
For Research Use Only. Not for use in diagnostic procedures
Highly purified human C3 was isolated from normal serum and used to immunize goats. The Anti-Human C3 Polyclonal Antisera was tested against normal human plasma by double immunodiffusion, one-dimensional immunoelectrophoresis, quantitative radial immunodifussion, and quantitative rocket immunoelectrophoresis. The antiserum was determined to be monospecific for C3 at varying concentrations.
C3 plays a central role for the classical, alternative, and lectin pathways of the complement system. The circulating form of C3 is naturally glycosylated and contains two disulfide-bonded chains that weigh approximately 110 kD and 75 kD, respectively. The average concentration of circulating C3 in human serum/plasma is 1.25 mg/mL.
Activation of any of the three complement pathways results in the cleavage of C3 into C3a and C3b fragments. C3a is one of the three complement-derived anaphylatoxins. The C3a polypeptide also exhibits immunoregulatory activity. This activity is dependent on the physical binding of C3a to helper T lymphocytes, which results in the inhibition of helper T cell function.
Applications of the C3 polyclonal antisera have been evaluated by various research facilities, and include Western Blot, 1 Flow Cytometry, 2 IHC, 3 Immunoblot, 4 and ELISA. 5
1、Wright, A., Morrison, S. Effect of C2 Associated Carbohydrate structure of Ig Effector function: studies with chimeric mouse human IgG1 Antibodies in glycosylation mutants of chinese hamster ovary cells, J. Immunol 160:3393-3402, 1998.
2、Walsh, M., Murray, J. Dual Implication of 2'3' Cyclic Nucleotide 3' Phosphodiesterase as a Major AutoAntigen and C3 Complement binding Protein in the Pathogenesis of Multiple Sclerosis, J. Clin Invest 101(9) 1923-1931, 1998.
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