84-1219-80 ALMS1 (Alstrom Syndrome Protein 1, KIAA0328) 100ug A1359-01B
特徴
- This protein contains a large tandem-repeat domain that contains no cysteine residues.
- Mutations in this gene have been associated with Alstrom syndrome.
- The encoded protein may play a role in hearing, sight, obesity, and liver function.
- Alternative splice variants have been described but their full length sequences have not been determined.
- Applications:Suitable for use in ELISA and Immunohistochemistry.
- Other applications not tested.
- Recommended Dilution:ELISA: 1:32,000Immunohistochemistry (Paraffin): 1-3ug/mlOptimal 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 at least 12 months.
- For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
仕様
- Size：100ug
- Host：goat
- Source Antibody：human
- Grade：Affinity Purified
- Purity：Purified by immunoaffinity chromatography.
- Form：Supplied as a liquid in Tris saline, 0.02% sodium azide, pH 7.3, 0.5% BSA.
- Specificity：Recognizes human ALMS1. Species sequence homology: Bovine, canine, mouse and rat.
- Isotype：IgG
- Calc Applications Abbrev：E IHC
- Calc Crossreactivity：Bo Ca Hu Mo Rt
- Immunogen：Synthetic peptide corresponding to C-RVTNQLLGRKVPWD, from human ALMS1, at C-terminal (NP_055935.4).
- Shelf Life：1year
- EU Commodity Code：30021010
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