MABF1978

Anti-Complement C3a/C3a (desArg) Antibody, clone K13/16

clone K13/16, from mouse

Manufacturer: Sigma Aldrich

Synonym(S): Complement C3a, C3 and PZP-like alpha-2-macroglobulin domain-containing protein 1

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Pack Size SKU Availability Price
200 μL MABF1978-200-μL In Stock ₹ 36,880.00

MABF1978 - 200 μL

₹ 36,880.00

In Stock

Quantity

1

Base Price: ₹ 36,880.00

GST (18%): ₹ 6,638.40

Total Price: ₹ 43,518.40

biological source

mouse

Quality Level

100

antibody form

purified antibody

antibody product type

primary antibodies

clone

K13/16, monoclonal

species reactivity

human

packaging

antibody small pack of 25 μL

technique(s)

flow cytometry: suitableimmunohistochemistry: suitable (paraffin)neutralization: suitable

isotype

IgG1κ

NCBI accession no.

NP_000055

Description

  • General description: Complement C3 (UniProt: P01024; also known as C3 and PZP-like alpha-2-macroglobulin domain-containing protein 1) is encoded by the C3 (also known as CPAMD1) gene (Gene ID: 718) in human. C3 is a secreted protein that plays a key role in the activation of the complement system. It s processing by C3 convertase is the central reaction in both classical and alternative complement pathways. C3 has an anaphylatoxon-like domain (aa 693-728) and a NTR (Netrin) domain (aa 1518-1661). IC3 precursor is first processed by the removal of four Arginine residues, forming two chains, beta and alpha, linked by a disulfide bond. C3 convertase activates C3 by cleaving the alpha chain, releasing C3a anaphylatoxin and generating C3b. C3a appears to be important in many inflammatory respons-es and the C3b fragment covalently binds to the cell or bacterial surface and plays a role in opsonisation. C3a anaphylatoxin is a mediator of local inflammatory process. In chronic inflammation, it acts as a chemoattractant for neutrophils. Defects in C3 gene can cause complement component 3 deficiency that leads to recurrent, severe, pyogenic infections because of ineffective opsonization of pathogens. Defects in C3 gene also cause age-related macular degeneration and hemolytic uremic syndrome that can lead to hemolytic anemia and renal failure
  • Specificity: Clone K13/16 recognizes complement C3a in human tissues. It targets an epitope that is present on human C3, C3a, and C3a-desArg.
  • Immunogen: A full length native C3a fragment purified from human serum that was activated at 37°C for 1 hour by treatment with 10 mg/mL zymosan.
  • Application: Anti-Complement C3a/C3a (desArg), clone K13/16, Cat. No. MABF1978, is a mouse monoclonal antibody that detects Complement C3a and has been tested for use in Flow Cytometry, Immunohistochemistry (Paraffin), Neutralization, and Agonist and Inhibition studies.
  • Quality: Evaluated by Immunohistochemistry in human kidney tissue.Immunohistochemistry Analysis: A 1:50 dilution of this antibody detected Complement C3a/C3a (desArg) in human kidney tissue sections.
  • Target description: 187.15 kDa calculated.
  • Physical form: Format: Purified
  • Storage and Stability: Stable for 1 year at 2-8°C from date of receipt.
  • Other Notes: Concentration: Please refer to lot specific datasheet.
  • Disclaimer: Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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