84-3440-06 ［取扱停止］BBS4, ID (Bardet-Biedl Syndrome 4 Protein) (AP) 200ul B2641-01-AP
特徴
- BBS4 contains tetratricopeptide repeats (TPR), similar to O-linked N-acetyglucosamine transferase.
- Mutations in the gene encoding this protein have been observed in patients with Bardet-Biedl syndrome type 4.
- BBS4 may play a role in pigmentary retinopathy, obesity, polydactyly, renal malformation and mental retardation.
- Applications:Suitable for use in ELISA and Western Blot.
- Other applications not tested.
- Recommended Dilution:ELISA: 1:1,000Western Blot: 1:50-1:100Optimal dilutions to be determined by the researcher.
- Storage and Stability:Store product at 4°C.
- DO NOT FREEZE! Stable at 4°C for 12 months after receipt as an undiluted liquid.
- Dilute required amount only prior to immediate use.
- Further dilutions can be made in assay buffer.
- For maximum recovery of product, centrifuge the original vial prior to removing the cap.
- Note: Applications are based on unconjugated antibody.
仕様
- Size：200ul
- Host：rabbit
- Source Antibody：human
- Grade：Purified
- Purity：Purified by ammonium sulfate precipitation.
- Form：Supplied as a liquid in PBS, pH 7.2. No preservative added. Labeled with Alkaline Phosphatase.
- Specificity：Recognizes human BBS4.
- Isotype：IgG
- Calc Applications Abbrev：E WB
- Calc Crossreactivity：Hu
- Immunogen：Synthetic peptide selected from the Center region of human BBS4 (KLH).
- Shelf Life：1year
- Swiss Prot Number：Q96RK4
- EU Commodity Code：30021010
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