TINF2 anticorps (AA 40-120)
Aperçu rapide pour TINF2 anticorps (AA 40-120) (ABIN7220998)
Antigène
Voir toutes TINF2 (TIN2) AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 40-120
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Fonction
- TIN2 Polyclonal Antibody
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Specificité
- TIN2 Polyclonal Antibody detects endogenous levels of TIN2 protein.
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Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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Immunogène
- Synthesized peptide derived from the Internal region of human TIN2 at AA range: 40-120
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Isotype
- IgG
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Indications d'application
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), IHC-P (1:100-1:300), ELISA (1:10000). Not yet tested in other applications.
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Commentaires
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Primary Antibody
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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
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: 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
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- TINF2 (TIN2) (TERF1 Interacting Nuclear Factor 2 (TIN2))
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Autre désignation
- TIN2
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Sujet
- Rabbit Anti-TIN2 Polyclonal Antibody,TINF2, TIN2, TERF1-interacting nuclear factor 2, TRF1-interacting nuclear protein 2,TINF2 encodes one of the proteins of the shelterin, or telosome, complex which protects telomeres by allowing the cell to distinguish between telomeres and regions of DNA damage. The TERF1 interacting nuclear factor 2 encoded by TINF2 is a critical part of shelterin, it interacts with the three DNA-binding proteins of the shelterin complex, and it is important for assembly of the complex. Mutations in this gene cause dyskeratosis congenita (DKC), an inherited bone marrow failure syndrome.,TERF1-interacting nuclear factor 2
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Poids moléculaire
- observerd band 53kDa
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ID gène
- 26277
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UniProt
- Q9BSI4
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Pathways
- Cycle Cellulaire, Telomere Maintenance, Regulation of Carbohydrate Metabolic Process
Antigène
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