BM2137 Lipoprotein (a) (Lp (a)) antibody

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Mouse anti Human Lipoprotein (a) (Lp (a)) 12C11.D5


Product Description for Lipoprotein (a) (Lp (a))

Mouse anti Human Lipoprotein (a) (Lp (a)) 12C11.D5.
Presentation: Purified
Product is tested for Enzyme Immunoassay, Western blot / Immunoblot.

Properties for Lipoprotein (a) (Lp (a))

Product Category Primary Antibodies
Quantity 0.5 mg
Presentation Purified
Reactivity Hu
Applications E, WB
Clonality Monoclonal
Clone 12C11.D5
Host Mouse
Isotype IgG1
Shipping to Worldwide
PDF datasheet View Datasheet
Manufacturer Acris Antibodies GmbH
Material safety datasheet MSDS for Monoclonal Antibodies (de)

Datasheet Extract

Purified lipoprotein(a) [Lp(a)] isolated from human plasma separated on a potassium bromide gradient (1.063-1.21 g/ml fraction) and followed by gel filtration chromatography.
Isotype control AM03095PU-N, SM10P (for use in human samples)
Application Can be used in research studies to identify Apo(a) in Lp(a) present in human plasma or serum using a capture ELISA or to identify purified Apo(a) (purified by native gel electrophoresis) in Western blot analysis.
Concentration 1.0 mg/ml (BCA method)
General Readings
  1. DeBacker, G., Rosseneu, M., DeSlypere, J.P. (1982) Atjerpsc;erpsos 42:197.
  2. The Lipid Research Clinics Primary Prevention Trial Results. (1984) J. Am. Med. Assoc. 251:351.
  3. DeBacker, G., Hulstaert, F., DeMunck, K., Rosseneu, M., Van Parijs, L., Dramaix, M. (1986) Am. Heart Journal 112:478.
  4. Laemmli, V., (1970), Nature, 227:680.
Storage Store the antibody undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer.
Avoid repeated freezing and thawing.
Shelf life: one year from despatch.
Protein A chromatography and 0.22 µm filteration.
Buffer System:
PBS buffer, pH 7.0 with 0.09% Sodium Azide as preservative.
Liquid purified Ig fraction (>95% pure)
Binds in ELISA (both indirect and sandwich) to native APO (a) in Lp(a) and shows no cross-reactivity with other apolipoproteins or plasminogen.
All isoforms of human Apo(a) are recognized.
This specificity was confirmed by Western blot analysis (native agarose gels) using a peroxidase-labeled secondary antibody and diaminobenzidine substrate.

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