Mast Cell Tryptase (HRP)

Cat# M2415-02C-HRP-100ul

Size : 100ul

Brand : US Biological

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M2415-02C-HRP Mast Cell Tryptase (HRP)

Clone Type
Polyclonal
Host
mouse
Source
human
Isotype
IgG1
Grade
Affinity Purified
Applications
E IHC WB
Crossreactivity
Ca Fe Hu Mk Rt
Shipping Temp
Blue Ice
Storage Temp
-20°C

Mast cells contain a number of preformed chemical mediators such as histamine, chymase, carboxypeptidase and proteolytic tryptase. A substantial quantity of tryptase is estimated to be found in mast cells of skin and lung and suggestes this enzyme plays a major role in mast cell mediated events. In vitro studies indicate tryptase can cleave C3 to form C3a anaphylatoxin, inactivate fibrinogen as a coaguable substrate for thrombin and activate latent collagenase. Human mast cell tryptase has considerable potential as a marker for mast cell activation as well as being a mediator of inflammation. ||Applications: |Suitable for use in ELISA, Western Blot and Immunohistochemistry. Other applications have not been tested. ||Recommended Dilutions:|Immunohistochemistry: Frozen sections|Immunohistochemistry (Paraffin): Requires antigen retrieval using heat treatment prior to staining paraffin sections. Sodium citrate buffer pH 6.0 is recommended. |Optimal dilutions to be determined by the researcher.||Hybridoma: |NS1 myeloma cells with spleen cells from Balb/c mice.||Immunohistochemistry Positive Control Tissue:|Tonsil||Storage and Stability:|Store product at 4°C if to be used immediately within two weeks. For long-term storage, aliquot to avoid repeated freezing and thawing and store at -20°C. Aliquots are stable at -20°C for 12 months after receipt. Dilute required amount only prior to immediate use. Further dilutions can be made in assay buffer. Note: Sodium azide is a potent inhibitor of peroxidase and should not be added to HRP conjugates. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.||Note: Applications are based on unconjugated antibody.

Applications
Product Type: Mab|Isotype: IgG1|Clone No: 3H2643 (AA1)|Host: mouse|Source: human|Concentration: As Reported|Form: Supplied as a liquid in PBS, pH 7.2. Labeled with Horseradish peroxidase (HRP).|Purity: Purified by Protein G affinity chromatography from tissue culture supernatant.|Immunogen: Human mast cell tryptase purified from human lung tissue.|Specificity: Recognizes human Mast Cell Tryptase, both alpha and beta isoforms. This antibody is an excellent marker for mast cells and does not bind to any other cell type in Immunohistochemistry. Species Crossreactivity: canine, feline, monkey and rat.||Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.
Immunogen
Human mast cell tryptase purified from human lung tissue.
Form
Supplied as a liquid in PBS, pH 7.2. Labeled with Horseradish peroxidase (HRP).
Purity
Purified by Protein G affinity chromatography from tissue culture supernatant.
Specificity
Recognizes human Mast Cell Tryptase, both alpha and beta isoforms. This antibody is an excellent marker for mast cells and does not bind to any other cell type in Immunohistochemistry. Species Crossreactivity: canine, feline, monkey and rat.
References
1. Walls, A.F., et al., J. Pathol. 162: 119-126 (1990). 2. Walls, A.F., et al., Clin. Exp. Allergy 20: 581-589 (1990). 3. Ozaki, K., et al., Vet. Pathol. 39: 557-564 (2002). 4. Louiset, E. et al. (2008) Endocr Relat Cancer. 15: 1025-34. 5. Xiang, M. et al. (2011) Usefulness of Serum Tryptase Level as an Independent Biomarker for Coronary Plaque Instability in a Chinese Population Atherosclerosis Jan 26 [Epub before print]. 6. Jacob, C. et al. (2005) J Biol Chem. 280: 31936-48. 7. Mauro, L.V. et al. (2008) Mol Med Report. 1: 895-902. 8. Liu, J. et al. (2009) Nat Med. 15: 940-5. 9. Asano-Kato, N. et al. (2005) Invest Ophthalmol Vis Sci. 46: 4622-6. 10. Facoetti, A. et al. (2006) Eur J Histochem. 50: 133-40. 11. Thienemann, F. et al. (2004) Arch Dermatol Res. 296: 134-8.