IgE, Heavy Chain

Referencia I1900-65-250ug

embalaje : 250ug

Marca : US Biological

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I1900-65 IgE, Heavy Chain

Clone Type
Polyclonal
Host
mouse
Source
rat
Swiss Prot
P01855
Isotype
IgG1
Grade
Affinity Purified
Applications
E WB
Crossreactivity
Rt
Shipping Temp
Blue Ice
Storage Temp
-20°C

Applications:|Suitable for use in ELISA and Western Blot. Other applications have not been tested||Recommended Dilutions:|ELISA: 5ug/ml as coating antibody|Optimal working dilutions to be determined by researcher.||Hybridoma: |Spleen cells from immunized BALB/c mice fused with mouse SP2/0 myeloma cells||Recommended Pair:|Coating: I1900-65|Detection: K0100-01 with I1900-55||Storage and Stability:|May be stored at 4°C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Aliquots are stable for 12 months after receipt. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.

Applications
Product Type: Mab|Isotype: IgG1|Clone No: 3H2277 (MARE-1)|Host: mouse|Source: rat|Concentration: ~1mg/ml|Form: Supplied as a liquid in PBS, pH 7.4, 0.09% sodium azide.|Purity: Purified by Protein G affinity chromatography from tissue culture supernatant.|Immunogen: Rat IR162, IR1016, IR2 and IR410 IgE myeloma proteins.|Specificity: Recognizes the epsilon chain of rat IgE. Does not cross-react with other classes of rat immunoglobulin. ||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
Rat IR162, IR1016, IR2 and IR410 IgE myeloma proteins.
Form
Supplied as a liquid in PBS, pH 7.4, 0.09% sodium azide.
Purity
Purified by Protein G affinity chromatography from tissue culture supernatant.
Specificity
Recognizes the epsilon chain of rat IgE. Does not cross-react with other classes of rat immunoglobulin.
References
1. Bazin H, et al. 1987. J. Immunol. 121: 2077-2081. 2. Bazin H, et al. 1984. J. Imm. Methods. 71: 9-16. 3. Bazin H, et al. 1984. J. Imm. Methods. 66: 261-269.