T-Box 1 antibody (AA 280-360)
Quick Overview for T-Box 1 antibody (AA 280-360) (ABIN7217242)
Target
See all T-Box 1 (TBX1) AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 280-360
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Purpose
- TBX1 Polyclonal Antibody
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Specificity
- TBX1 Polyclonal Antibody detects endogenous levels of TBX1 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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Immunogen
- Synthesized peptide derived from the C-terminal region of human TBX1 at AA range: 280-360
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Isotype
- IgG
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Application Notes
- 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), IF (1:200-1:1000), ELISA (1:20000). Not yet tested in other applications.
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Comment
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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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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- 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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- T-Box 1 (TBX1)
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Alternative Name
- TBX1
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Background
- Rabbit Anti-TBX1 Polyclonal Antibody,TBX1, T-box transcription factor TBX1, T-box protein 1, Testis-specific T-box protein,TBX1 is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This gene product shares 98 % amino acid sequence identity with the mouse ortholog. DiGeorge syndrome (DGS)/velocardiofacial syndrome (VCFS), a common congenital disorder characterized by neural-crest-related developmental defects, has been associated with deletions of chromosome 22q11. , where this gene has been mapped. Studies using mouse models of DiGeorge syndrome suggest a major role for this gene in the molecular etiology of DGS/VCFS. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene.,T-box transcription factor TBX1
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Molecular Weight
- observerd band 43kDa
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Gene ID
- 6899
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UniProt
- O43435
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Pathways
- Retinoic Acid Receptor Signaling Pathway, Sensory Perception of Sound, Cellular Response to Molecule of Bacterial Origin, Regulation of Muscle Cell Differentiation
Target
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