HINT1 anticorps (AA 40-120)
Aperçu rapide pour HINT1 anticorps (AA 40-120) (ABIN7221490)
Antigène
Voir toutes HINT1 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 40-120
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Fonction
- Rabbit Anti-Hint1 Polyclonal Antibody
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Specificité
- Hint1 Polyclonal Antibody detects endogenous levels of Hint1 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 Hint1 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 1:100-1:300,IF 1:200-1:1000,ELISA 1:20000,Not yet tested in other applications.
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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
- Liquid in 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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Date de péremption
- 12 months
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- HINT1 (Histidine Triad Nucleotide Binding Protein 1 (HINT1))
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Autre désignation
- Hint1
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Sujet
- HINT1, HINT, PKCI1, PRKCNH1, Histidine triad nucleotide-binding protein 1, Adenosine 5'-monophosphoramidase, Protein kinase C inhibitor 1, Protein kinase C-interacting protein 1, PKCI-1HINT1 encodes histidine triad nucleotide binding protein 1 that hydrolyzes purine nucleotide phosphoramidates substrates, including AMP-morpholidate, AMP-N-alanine methyl ester, AMP-alpha-acetyl lysine methyl ester, and AMP-NH2. The encoded protein interacts with these substrates via a histidine triad motif. This gene is considered a tumor suppressor gene. In addition, mutations in this gene can cause autosomal recessive neuromyotonia and axonal neuropathy. There are several related pseudogenes on chromosome 7. Several transcript variants have been observed.
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Poids moléculaire
- 28kD
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ID gène
- 3094
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UniProt
- P49773
Antigène
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