IgA, alpha
Katalog-Nummer I1890-05D-2mg
Size : 2mg
Marke : US Biological
I1890-05D IgA, alpha
Clone Type
PolyclonalHost
rabbitSource
humanIsotype
IgGGrade
Affinity PurifiedApplications
E IHC WBCrossreactivity
HuShipping Temp
Blue IceStorage Temp
4°C (-20°C Glycerol)Applications: |Suitable for use in ELISA, Western Blot and Immunohistochemistry. Other applications not tested.||Recommended Dilution: |ELISA : 1:5,000 - 1:20,000|Western Blot : 1:500 - 1:2,000|Immunohistochemistry: 1:1,000 - 1:5,000|Optimal dilutions to be determined by the researcher.||Storage and Stability:|May be stored at 4°C for short-term only. For long-term storage, store at -20°C. Aliquots are stable for at least 12 months at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer.
Applications
Product Type: Pab|Isotype: IgG|Host: rabbit|Source: human|Concentration: ~1mg/ml|Form: Supplied as a liquid in PBS pH 7.2, 0.01% sodium azide, before the addition of glycerol to 40%.|Purity: Purified by immunoaffinity chromatography using Human IgA coupled to agarose followed by solid phase adsorption(s).|Immunogen: Human IgA alpha heavy chain|Specificity: Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Rabbit Serum, Human IgA and Human Serum. No reaction was observed against other human heavy or light chain proteins.||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 IgA alpha heavy chain
Form
Supplied as a liquid in PBS pH 7.2, 0.01% sodium azide, before the addition of glycerol to 40%.
Purity
Purified by immunoaffinity chromatography using Human IgA coupled to agarose followed by solid phase adsorption(s).
Specificity
Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Rabbit Serum, Human IgA and Human Serum. No reaction was observed against other human heavy or light chain proteins.
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