C9orf6 anticorps (AA 1-100) (AbBy Fluor® 350)
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- Antigène Voir toutes C9orf6 (FAM206A) Anticorps
- C9orf6 (FAM206A) (Family with Sequence Similarity 206, Member A (FAM206A))
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Épitope
- AA 1-100
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Reactivité
- Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp C9orf6 est conjugé à/à la AbBy Fluor® 350
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Application
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Réactivité croisée
- Rat
- Homologie
- Human,Mouse,Dog,Cow,Sheep,Pig,Horse
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human C9orf6
- Isotype
- IgG
- Top Product
- Discover our top product FAM206A 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
- C9orf6 (FAM206A) (Family with Sequence Similarity 206, Member A (FAM206A))
- Autre désignation
- C9orf6 (FAM206A Produits)
- Synonymes
- anticorps Fam206a, anticorps C9orf6, anticorps CG-8, anticorps C8H9orf6, anticorps C2H9orf6, anticorps si:ch211-254e15.2, anticorps zgc:153072, anticorps family with sequence similarity 206, member A, anticorps family with sequence similarity 206 member A, anticorps Fam206a, anticorps FAM206A, anticorps fam206a
- Sujet
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Synonyms: CG 8, CG8, FLJ20457, Hypothetical protein LOC54942, UPF0436 protein C9orf6, F206A_HUMAN.
Background: Chromosome 9 consists of about 145 million bases and 4 % of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf6 gene product has been provisionally designated C9orf6 pending further characterization.
- ID gène
- 54942
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