ZNF503 anticorps (AA 41-140) (Cy5)
Aperçu rapide pour ZNF503 anticorps (AA 41-140) (Cy5) (ABIN1704365)
Antigène
Voir toutes ZNF503 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 41-140
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Réactivité croisée
- Souris
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Homologie
- Human,Rat,Dog,Cow,Pig,Horse,Chicken
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Purification
- Purified by Protein A.
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Immunogène
- KLH conjugated synthetic peptide derived from human ZNF503/NOLZ1
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Isotype
- IgG
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Indications d'application
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 -
Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 μg/μL
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Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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Agent conservateur
- ProClin
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Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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Stock
- -20 °C
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Stockage commentaire
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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Date de péremption
- 12 months
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- ZNF503 (Zinc Finger Protein 503 (ZNF503))
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Autre désignation
- ZNF503/NOLZ1
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Sujet
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Synonyms: FLJ45745, MGC2555, NOLZ 1, NOLZ1, Zinc finger protein 503, ZN503_HUMAN, znf503.
Background: Nolz 1 is a 646 amino acid nuclear protein that is thought to function as a transcriptional repressor and is highly expressed in developing striatum. Additionally, Nolz-1 has been suggested to play a role in neural differentiation. A member of the Elbow/Noc family, Nolz-1 exists as three alternatively spliced isoforms and contains one C2H2-type zinc finger. The gene encoding Nolz-1 maps to human chromosome 10, which makes up approximately 4.5 % of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman?s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
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ID gène
- 84858
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UniProt
- Q96F45
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Pathways
- SARS-CoV-2 Protein Interactome
Antigène
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