FIGNL1 anticorps (Cy7)
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- Antigène Voir toutes FIGNL1 Anticorps
- FIGNL1 (Fidgetin-Like 1 (FIGNL1))
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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 FIGNL1 est conjugé à/à la Cy7
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Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Réactivité croisée
- Humain, Souris, Rat
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human FIGNL1
- Isotype
- IgG
- Top Product
- Discover our top product FIGNL1 Anticorps primaire
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- Indications d'application
- 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 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Date de péremption
- 12 months
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- Antigène
- FIGNL1 (Fidgetin-Like 1 (FIGNL1))
- Autre désignation
- FIGNL1 (FIGNL1 Produits)
- Synonymes
- anticorps fb82h05, anticorps wu:fb82h05, anticorps wu:fj99a11, anticorps zgc:193664, anticorps fidgetin like 1, anticorps fidgetin-like 1, anticorps fidgetin-like 1 L homeolog, anticorps FIGNL1, anticorps fignl1, anticorps Fignl1, anticorps fignl1.L
- Sujet
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Synonyms: Fidgetin like protein 1, fidgetin-like 1, FIGL1_HUMAN.
Background: FIGNL1 is a 674 amino acid protein belonging to the AAA ATPase family. FIGNL1 exists as a hexamer that undergoes alternative splicing to produce two isoforms. FIGNL1 utilizes magnesium as a cofactor and is phosphorylated upon DNA damage, probably by ATM or ATR. FIGNL1 is suggested to regulate osteoblast proliferation and differentiation. FIGNL1 is encoded by a gene located on human chromosome 7, which consists about 158 milllion bases, encodes over 1000 genes and makes up about 5 % of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
- ID gène
- 63979
- Pathways
- Dynamique des Microtubules
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