FOPNL anticorps (AA 6-80) (Cy5)
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- Antigène Voir toutes FOPNL Anticorps
- FOPNL (FGFR1OP N-Terminal Like (FOPNL))
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Épitope
- AA 6-80
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Reactivité
- Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp FOPNL est conjugé à/à la Cy5
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Application
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Réactivité croisée
- Souris, Rat
- Homologie
- Human,Dog,Cow,Sheep,Pig,Horse
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human FOPNL/C16orf63
- Isotype
- IgG
- Top Product
- Discover our top product FOPNL Anticorps primaire
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- Indications d'application
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 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
- FOPNL (FGFR1OP N-Terminal Like (FOPNL))
- Autre désignation
- FOPNL/C16orf63 (FOPNL Produits)
- Synonymes
- anticorps C16orf63, anticorps FOR20, anticorps PHSECRG2, anticorps C14H16orf63, anticorps 0610037P05Rik, anticorps FGFR1OP N-terminal like, anticorps Fgfr1op N-terminal like, anticorps FGFR1OP N-terminal like L homeolog, anticorps FOPNL, anticorps Fopnl, anticorps fopnl.L
- Sujet
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Synonyms: C16orf63, FGFR1OP N terminal like, FGFR1OP N-terminal-like protein, FOP-related protein of 20 kDa, Fopnl, FOPNL_HUMAN, FOR20, LisH domain containing protein C16orf63, LisH domain-containing protein FOPNL, PHSECRG2, Pluripotent embryonic stem cell related protein.
Background: C16orf63, also known as FLJ31153 or DKFZp686N1651, is a 174 amino acid protein that contains one LisH domain. The gene that encodes C16orf63 maps to human chromosome 16. Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3 % of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier. The C16orf63 gene product has been provisionally designated C16orf63 pending further characterization.
- ID gène
- 123811
- Pathways
- Maintenance of Protein Location
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