FANCG anticorps (pSer383) (Biotin)
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- Antigène Voir toutes FANCG Anticorps
- FANCG (Fanconi Anemia Complementation Group G (FANCG))
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Épitope
- pSer383
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp FANCG est conjugé à/à la Biotin
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Application
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- Homologie
- Human,Mouse,Rat
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic phosphopeptide derived from human FANCG around the phosphorylation site of Ser383
- Isotype
- IgG
- Top Product
- Discover our top product FANCG Anticorps primaire
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- Indications d'application
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Agent conservateur
- ProClin
- Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C for 12 months.
- Date de péremption
- 12 months
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- Antigène
- FANCG (Fanconi Anemia Complementation Group G (FANCG))
- Autre désignation
- FANCG (FANCG Produits)
- Synonymes
- anticorps xFANCG, anticorps FAG, anticorps XRCC9, anticorps AU041407, anticorps Xrcc9, anticorps Fanconi anemia complementation group G S homeolog, anticorps Fanconi anemia complementation group G, anticorps Fanconi anemia, complementation group G, anticorps fancg.S, anticorps FANCG, anticorps Fancg
- Sujet
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Synonyms: FANCG phospho S383, p-FANCG phospho S383, DNA repair protein XRCC9, DNA-repair protein XRCC9, FAG, Fanconi anaemia complementation group G, Protein FACG, X ray repair, complementing defective, in Chinese hamster cells 9, XRCC9.
Background: FANCG, involved in Fanconi anemia, confers resistance to both hygromycin and mitomycin C. FANCG contains a 5-prime GC-rich untranslated region characteristic of housekeeping genes. The putative 622-amino acid protein has a leucine-zipper motif at its N-terminus. Fanconi anemia is an autosomal recessive disorder with diverse clinical symptoms, including developmental anomalies, bone marrow failure, and early occurrence of malignancies. A minimum of 8 FA genes have been identified.
- ID gène
- 2189
- Pathways
- Réparation de l'ADN
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