84-4336-91 ABHDB, ID (ABHD11, WBSCR21, Abhydrolase domain-containing protein 11, Williams-Beuren syndrome chromosomal region 21 protein) 100ul 304186
特徴
- This gene encodes a protein containing an alpha/beta hydrolase fold domain.
- This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.
- Alternatively spliced transcript variants have been described, but their biological validity has not been determined.
- Applications:Suitable for use in Western Blot.
- Other applications not tested.
- Recommended Dilution:Western Blot: 1:500-1:3000Optimal 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：100ul
- Host：rabbit
- Source Antibody：human
- Grade：Affinity Purified
- Purity：Purified by immunoaffinity chromatography.
- Form：Supplied as a liquid in PBS, pH 7.4, 150mM sodium chloride, 0.02% sodium azide, 50% glycerol.
- Specificity：Recognizes human ABHD11.
- Isotype：IgG
- Calc Applications Abbrev：WB
- Calc Crossreactivity：Hu
- Immunogen：Synthetic peptide corresponding to internal of human ABHD11.
- Shelf Life：1year
- Swiss Prot Number：Q8NFV4
- EU Commodity Code：30021010
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