FANCM anticorps
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- Antigène Voir toutes FANCM Anticorps
- FANCM (Fanconi Anemia Complementation Group M (FANCM))
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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 FANCM est non-conjugé
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Application
- Immunofluorescence (IF)
- Purification
- Affinity purification
- Immunogène
- Recombinant fusion protein of human FANCM (NP_065988.1).
- Isotype
- IgG
- Top Product
- Discover our top product FANCM Anticorps primaire
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- Indications d'application
- IF 1:50-1:100
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 mg/mL
- Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- 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. Avoid freeze / thaw cycles.
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- Antigène
- FANCM (Fanconi Anemia Complementation Group M (FANCM))
- Autre désignation
- FANCM (FANCM Produits)
- Synonymes
- anticorps FAAP250, anticorps KIAA1596, anticorps AI427100, anticorps C730036B14Rik, anticorps D12Ertd364e, anticorps Fanconi anemia complementation group M, anticorps hypothetical protein, anticorps Fanconi anemia, complementation group M, anticorps FANCM, anticorps PGTG_17854, anticorps Fancm
- Sujet
- The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity, they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group M. Alternative splicing results in multiple transcript variants.
- Poids moléculaire
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Observed_MW: Refer to figures
Calculated_MW: 75kDa/229kDa/232kDa
- ID gène
- 57697
- UniProt
- Q8IYD8
- Pathways
- Réparation de l'ADN
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