ASXL1 anticorps (N-Term)
Aperçu rapide pour ASXL1 anticorps (N-Term) (ABIN7469244)
Antigène
Voir toutes ASXL1 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
Classe de qualité
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Épitope
- N-Term
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Specificité
- Knockdown/Knockout validation was supported by references (PMID:26385183)
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Réactivité croisée
- Humain, Souris
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Purification
- Purified by antigen-affinity chromatography.
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Immunogène
- Recombinant protein encompassing a sequence within the N-terminus region of human ASXL1. The exact sequence is proprietary.
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Isotype
- IgG
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Indications d'application
- WB: 1:1000-1:10000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
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Commentaires
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Positive Control: GFP-human ASXL1-transfected 293T cells Validation: KO/KD, Overexpression
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- 1XPBS ( pH 7), 20 % Glycerol, 0.01 % Thimerosal
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Agent conservateur
- Thimerosal (Merthiolate)
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Précaution d'utilisation
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- 4 °C,-20 °C
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Stockage commentaire
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- ASXL1 (Additional Sex Combs Like 1 (ASXL1))
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Autre désignation
- ASXL1
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Sujet
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Synonyms: ASXL transcriptional regulator 1 , BOPS , MDS
Background: This gene is similar to the Drosophila additional sex combs gene, which encodes a chromatin-binding protein required for normal determination of segment identity in the developing embryo. The protein is a member of the Polycomb group of proteins, which are necessary for the maintenance of stable repression of homeotic and other loci. The protein is thought to disrupt chromatin in localized areas, enhancing transcription of certain genes while repressing the transcription of other genes. The protein encoded by this gene functions as a ligand-dependent co-activator for retinoic acid receptor in cooperation with nuclear receptor coactivator 1. Mutations in this gene are associated with myelodysplastic syndromes and chronic myelomonocytic leukemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq]
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Poids moléculaire
- 165 kDa
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ID gène
- 171023
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UniProt
- Q8IXJ9
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Pathways
- Retinoic Acid Receptor Signaling Pathway
Antigène
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