GTF2I anticorps (pTyr248)
Aperçu rapide pour GTF2I anticorps (pTyr248) (ABIN7221394)
Antigène
Voir toutes GTF2I AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- pTyr248
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Fonction
- TFII-I (phospho Tyr248) Polyclonal Antibody
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Specificité
- Phospho-TFII-I (Y248) Polyclonal Antibody detects endogenous levels of TFII-I protein only when phosphorylated at Y248.
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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 human TFII-I Phospho-Tyr248
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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), ELISA (1:5000). 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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- GTF2I (General Transcription Factor III (GTF2I))
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Autre désignation
- TFII-I
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Sujet
- Rabbit Anti-TFII-I (phospho Tyr248) Polyclonal Antibody,GTF2I, BAP135, WBSCR6, General transcription factor II-I, GTFII-I, TFII-I, Bruton tyrosine kinase-associated protein 135, BAP-135, BTK-associated protein 135, SRF-Phox1-interacting protein, SPIN, Williams-Beuren syndrome chromosomal region,GTF2I encodes a phosphoprotein containing six characteristic repeat motifs. The general transcription factor IIi binds to the initiator element (Inr) and E-box element in promoters and functions as a regulator of transcription. This locus, along with several other neighboring genes, is deleted in Williams-Beuren syndrome. There are many closely related genes and pseudogenes for this gene on chromosome 7. This gene also has pseudogenes on chromosomes 9, 13, and 21. Alternatively spliced transcript variants encoding multiple isoforms have been observed.,General transcription factor II-I
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Poids moléculaire
- observerd band 115kDa
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ID gène
- 2969
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UniProt
- P78347
Antigène
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