PHF6 anticorps (AA 37-309)
Aperçu rapide pour PHF6 anticorps (AA 37-309) (ABIN7601498)
Antigène
Voir toutes PHF6 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 37-309
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Fonction
- Anti-PHF6 Antibody
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Réactivité croisée (Details)
- No cross reactivity with other proteins.
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Homologie
- Human PHF6 shares 98.2% amino acid (aa) sequence identity with mouse PHF6.
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Attributs du produit
- Anti-PHF6 Antibody. Tested in ELISA, IF, IHC, ICC, WB, Flow Cytometry applications. This antibody reacts with Human, Monkey, Mouse, Rat.
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Purification
- Immunogen affinity purified.
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Immunogène
- E.coli-derived human PHF6 recombinant protein (Position: Q37-D309). Human PHF6 shares 98.2% amino acid (aa) sequence identity with mouse PHF6.
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Isotype
- IgG
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Indications d'application
- Western blot, 0.25-0.5 μg/mL, Human, Monkey, Mouse, Rat Immunohistochemistry (Paraffin-embedded Section), 2-5 μg/mL, Human, Mouse, Rat Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human ELISA, 0.1-0.5 μg/mL, -
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
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Concentration
- 500 μg/mL
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Buffer
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
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Stock
- 4 °C,-20 °C
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Stockage commentaire
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At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing. -
Date de péremption
- 12 months
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- PHF6 (PHD Finger Protein 6 (PHF6))
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Autre désignation
- PHF6
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Sujet
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Background: PHD finger protein 6 is a protein that in humans is encoded by the PHF6 gene. 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 cognitive disability, epilepsy, hypogonadism, hypometabolism, obesity, swelling of subcutaneous tissue of the face, narrow palpebral fissures, and large ears. Alternate splicing results in multiple transcript variants, encoding different isoforms.
Gene Full Name: PHD finger protein 6
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Poids moléculaire
- 41 kDa
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ID gène
- 84295
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UniProt
- Q8IWS0
Antigène
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