PHD Finger Protein 6 (PHF6) Peptide
PHF6
Reactivité: Humain
Hôte: Synthetic
BP, WB
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- Antigène Tous les produits PHF6
- PHF6 (PHD Finger Protein 6 (PHF6))
- Origine
- Humain
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Attributs du produit
- This is a synthetic peptide designed for use in combination with anti-PHF6 antibody (Catalog #: ARP51235_T100). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- Purification
- Purified
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- Indications d'application
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Antigène
- PHF6 (PHD Finger Protein 6 (PHF6))
- Synonymes
- zgc:55403 Peptide, wu:fa22g03 Peptide, BFLS Peptide, BORJ Peptide, CENP-31 Peptide, 2700007B13Rik Peptide, 4931428F02Rik Peptide, mKIAA1823 Peptide, PHD finger protein 6 Peptide, PHD finger protein 6 L homeolog Peptide, phf6 Peptide, phf6.L Peptide, PHF6 Peptide, Phf6 Peptide
- Sujet
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PHF6 is a member of the plant homeodomain (PHD)-like finger (PHF) family. PHF6 is a protein with two PHD-type zinc finger domains, indicating a potential role in transcriptional regulation, that localizes to the nucleolus. Mutations affecting the coding region of its gene or the splicing of the transcript have been associated with Borjeson-Forssman-Lehmann syndrome (BFLS).This gene is a member of the plant homeodomain (PHD)-like finger (PHF) family. It encodes a protein with two PHD-type zinc finger domains, indicating a potential role in transcriptional regulation, that localizes to the nucleolus. Mutations affecting the coding region of this gene or the splicing of the transcript have been associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a disorder characterized by mental retardation, epilepsy, hypogonadism, hypometabolism, obesity, swelling of subcutaneous tissue of the face, narrow palpebral fissures, and large ears. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
Alias Symbols: BORJ, MGC14797, BFLS, CENP-31
Protein Size: 312 - Poids moléculaire
- 35 kDa
- ID gène
- 84295
- NCBI Accession
- NM_032335, NP_115711
- UniProt
- Q5JRC7
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