TNP1 antibody (AA 201-300) (AbBy Fluor® 680)
Quick Overview for TNP1 antibody (AA 201-300) (AbBy Fluor® 680) (ABIN6981192)
Target
See all TNP1 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 201-300
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Cross-Reactivity
- Human
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Predicted Reactivity
- Mouse,Rat,Dog,Cow,Sheep,Horse,Rabbit
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Purification
- Purified by Protein A.
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Immunogen
- KLH conjugated synthetic peptide derived from mouse Transition Protein 1
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Isotype
- IgG
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Application Notes
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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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Preservative
- ProClin
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Precaution of Use
- This product contains ProClin: 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
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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Expiry Date
- 12 months
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- TNP1 (Transition Protein 1 (During Histone To Protamine Replacement) (TNP1))
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Alternative Name
- Transition Protein 1
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Background
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Synonyms: 551G9.2, Anti Eukaryotic Release Factor 3a, Anti G1 to S phase transition 1, Anti GST1, homolog of yeast, eRF 3a, eRF3a, G1 to S phase transition 1, G1 to S phase transition protein 1 homolog, G1 to S phase transition protein, GSPT 1, GSPT1, GST 1, GST1, GTP binding protein GST1 HS, Transition protein 1, ERF3A_MOUSE.
Background: eRF3a is a 499 amino acid protein that belongs to the GTP-binding elongation factor family and is involved in the regulation of cell growth, specifically via control of translation termination. Human eRF3a shares 94 % sequence identity with its mouse counterpart, suggesting a conserved function between species. The gene encoding eRF3a maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3 % of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
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Gene ID
- 14852
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UniProt
- P15170
Target
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