84-4557-76 [取扱停止]HFE 20ul 389908
特徴
- The protein encoded by this gene is a membrane protein that is similar to MHC class I-type proteins and associates with beta2-microglobulin (beta2M).
- It is thought that this protein functions to regulate iron absorption by regulating the interaction of the transferrin receptor with transferrin.
- The iron storage disorder, hereditary haemochromatosis, is a recessive genetic disorder that results from defects in this gene.
- At least nine alternatively spliced variants have been described for this gene.
- Additional variants have been found but their full-length nature has not been determined.
- Applications:Suitable for use in Western Blot.
- Other applications not tested.
- Recommended Dilution:Western Blot: 1:500-1:2000Optimal dilutions to be determined by the researcher.
- 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.
仕様
- Size:20ul
- Host:rabbit
- Source Antibody:human
- Grade:Affinity Purified
- Purity:Purified by immunoaffinity chromatography.
- Form:Supplied as a liquid in PBS, pH 7.3, 0.05% sodium azide, 50% glycerol.
- Specificity:Recognizes human HFE. Species Crossreactivity: mouse and rat
- Isotype:IgG
- Calc Applications Abbrev:WB
- Calc Crossreactivity:Hu Mo Rt
- Immunogen:Recombinant protein corresponding to human HFE.
- Shelf Life:1year
- Swiss Prot Number:Q30201
- EU Commodity Code:30021010
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