TRIM29 anticorps (AA 253-283)
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- Antigène Voir toutes TRIM29 Anticorps
- TRIM29 (Tripartite Motif Containing 29 (TRIM29))
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Épitope
- AA 253-283
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Reactivité
- Humain, Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp TRIM29 est non-conjugé
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Application
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human TRIM29/ATDC
- Isotype
- IgG
- Top Product
- Discover our top product TRIM29 Anticorps primaire
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- Indications d'application
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WB 1:100-1000
IHC-P 1:100-500
IF(IHC-P) 1:50-200 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 1 % BSA, 50 % glycerol and 0.09 % sodium azide.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C
- Date de péremption
- 12 months
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- Antigène
- TRIM29 (Tripartite Motif Containing 29 (TRIM29))
- Autre désignation
- Trim29 (TRIM29 Produits)
- Synonymes
- anticorps ATDC, anticorps 1110047J21Rik, anticorps 2810431N19Rik, anticorps 4732461M22Rik, anticorps AI119726, anticorps MGC53484, anticorps TRIM29, anticorps atdc, anticorps tripartite motif containing 29, anticorps tripartite motif-containing 29, anticorps tripartite motif containing 29 L homeolog, anticorps TRIM29, anticorps Trim29, anticorps trim29.L, anticorps trim29
- Sujet
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It is able to complement the radiosensitivity defect of an ataxia telangiectasia (AT) fibroblast cell line.
Subcellular location: Helical
Synonyms: ATDC, Tripartite motif-containing protein 29, Ataxia telangiectasia group D-associated protein, TRIM29
- ID gène
- 23650
- UniProt
- Q14134
- Pathways
- Signalisation p53, Apoptose, Réparation de l'ADN, Inositol Metabolic Process, Positive Regulation of Response to DNA Damage Stimulus
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