Skip to Content
Merck
All Photos(1)

Key Documents

11815024001

Roche

Anti-Protein C Affinity Matrix

from mouse IgG1κ

Synonym(s):

affinity matrix, anti-protein c

Sign Into View Organizational & Contract Pricing


About This Item

UNSPSC Code:
12352203

biological source

mouse

Quality Level

conjugate

agarose conjugate

antibody form

purified immunoglobulin

clone

HPC4, monoclonal

form

slurry

packaging

pkg of 1 mL (settled resin volume)

manufacturer/tradename

Roche

isotype

IgG1, kappa

capacity

2-10 nmol/mL binding capacity

storage temp.

2-8°C

General description

Protein C is a Vitamin K-dependent plasma zymogen that is activated by proteolytic cleavage of the thrombin-thrombomodulin complex to form an anticoagulant enzyme. Anti-Protein C mouse monoclonal antibody (clone HPC4) binds specifically to an epitope sequence spanning the thrombin cleavage site of protein C and is immobilized. Anti-Protein C recognizes the 12-amino acid sequence (EDQVDPRLIDGK), which encodes residues 6 through 17 of the heavy chain of Protein C. The formation of the Anti-Protein C/protein C epitope complex is dependent on the presence of calcium ions. In the presence of Ca2+, the antibody binds with high affinity and specificity to this sequence in native human Protein C or in proteins tagged with this epitope. This efficient binding within the recombinant fusion protein occurs regardless of the site of incorporation of the epitope tag (i.e., N terminus, C terminus, or within the reading frame). This unique antibody is especially well suited for purification of recombinant fusion proteins tagged with the protein C epitope.

  • Insertion of the protein C tag does not introduce a new metal-ion binding site. The antibody contains the Ca2+ binding site.
  • Protein C tag can be integrated either at the N-terminus, C-terminus or internally without any change in antibody specificity.
  • Rapid immunoaffinity purification under non-denaturing conditions using economical calcium chelating agent (e.g., EDTA) or alternatively a specific protein C-tag peptide.

Monoclonal mouse antibody Anti-Protein C (clone HPC4) is covalently coupled to agarose beads. In the coupling reaction 4mg of antibody is reacted per 1ml of beads.

Specificity

Anti-Protein C recognizes the 12-amino acid sequence EDQVDPRLIDGK, which encodes residues 6 to 17 of the heavy chain of protein C. In the presence of Ca2, the antibody binds with high affinity and specificity to this sequence in native human protein C or in proteins tagged with this epitope. Efficient binding within the recombinant fusion protein occurs regardless of epitope position (N-terminal, C-terminal, or internal).

Application

Anti-Protein C Affinity Matrix is used for:
  • Immunoprecipitation of Protein C-tagged proteins from mammalian, bacterial, and yeast cell extracts
  • Affinity column purification of Protein C-tagged proteins from crude protein extracts

Following immunoprecipitation or purification, the tagged protein of interest may be analyzed by:
  • Western blotting using the Anti-Protein C antibody
  • Silver staining (or similar protein stain)

Features and Benefits

  • use gentle elution conditions using calcium-chelating agents like EDTA.
  • highly specific to EDQVDPRLIDGK, derived from protein C.
  • binding of Anti-Protein C to protein C-epitop is dependent on the presence of calcium ions.
  • suitable for purification of proteins containing protein C as N-terminal, C-terminal or internal fusion.
  • applicable with crued cell extracts from mammalian, bacterial, and yeast expression systems.

Contents
1. The antibody is covalently coupled to agarose beads and supplied as a 2ml slurry containing 1ml beads and 1ml buffer.
2. 4mg of antibody is reacted per ml of beads in the coupling reaction.
3. A plastic column with top and bottom caps is included.

Packaging

1 kit containing settled resin and column

Quality

Each lot of Anti-Protein C Affinity Matrix is tested for its ability to purify a Protein C-tagged protein expressed in transformed bacteria from crude bacterial extract. The antibody affinity column is used in combination with western blot and/or silver stain analysis.

Physical form

1 ml settled resin of Anti-Protein C Affinity Matrix in 20 mM Tris, 0.1 M NaCl, 1 mM CaCl2, and 0.09% sodium azide (w/v); 2 ml suspension equals to 1 ml bed volume. One plastic column with top and bottom caps is included

Analysis Note

KD = 10–9 M Binding Capacity is 2 to 10 nmol/ml affinity matrix. Yield of 10.5 nmol purified protein/ml affinity matrix was determined using a whole-cell bacterial extract containing protein C-tagged β-galactosidase.

Other Notes

For life science research only. Not for use in diagnostic procedures.

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point(F)

does not flash

Flash Point(C)

does not flash


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Arthur Günzl et al.
Eukaryotic cell, 2(3), 542-551 (2003-06-11)
In eukaryotes, RNA polymerase (pol) I exclusively transcribes the large rRNA gene unit (rDNA) and mRNA is synthesized by RNA pol II. The African trypanosome, Trypanosoma brucei, represents an exception to this rule. In this organism, transcription of genes encoding
Daniela Luz Ambrósio et al.
Eukaryotic cell, 8(7), 990-1000 (2009-05-12)
In trypanosomatid parasites, spliced leader (SL) trans splicing is an essential nuclear mRNA maturation step which caps mRNAs posttranscriptionally and, in conjunction with polyadenylation, resolves individual mRNAs from polycistronic precursors. While all trypanosomatid mRNAs are trans spliced, intron removal by
H Plun-Favreau et al.
The EMBO journal, 20(7), 1692-1703 (2001-04-04)
Ciliary neurotrophic factor (CNTF) is involved in the survival of a number of different neural cell types, including motor neurons. CNTF functional responses are mediated through a tripartite membrane receptor composed of two signalling receptor chains, gp130 and the leukaemia
Mary Anne T Rubio et al.
Nature, 542(7642), 494-497 (2017-02-24)
Nucleic acids undergo naturally occurring chemical modifications. Over 100 different modifications have been described and every position in the purine and pyrimidine bases can be modified; often the sugar is also modified. Despite recent progress, the mechanism for the biosynthesis
Jing Huang et al.
Journal of molecular and cellular cardiology, 66, 157-164 (2013-11-26)
Despite advances in the treatment of acute tissue ischemia significant challenges remain in effective cytoprotection from ischemic cell death. It has been documented that injected stem cells, such as mesenchymal stem cells (MSCs), can confer protection to ischemic tissue through

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service