C9orf163 anticorps (AA 101-203) (Biotin)
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- Antigène Tous les produits C9orf163 (C9ORF163)
- C9orf163 (C9ORF163) (Chromosome 9 Open Reading Frame 163 (C9ORF163))
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Épitope
- AA 101-203
- Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp C9orf163 est conjugé à/à la Biotin
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Application
- ELISA, Western Blotting (WB), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Homologie
- Human
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human C9orf163
- Isotype
- IgG
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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
- C9orf163 (C9ORF163) (Chromosome 9 Open Reading Frame 163 (C9ORF163))
- Autre désignation
- C9orf163 (C9ORF163 Produits)
- Synonymes
- anticorps RP11-413M3.11, anticorps chromosome 9 open reading frame 163, anticorps C9orf163
- Sujet
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Synonyms: C9orf163, Chromosome 9 open reading frame 163, CI163_HUMAN, FLJ36779, RP11-413M3.11, RP11-413M3.11-001, Uncharacterized protein C9orf163.
Background: C9orf163 (chromosome 9 open reading frame 163) is a 203 amino acid protein encoded by a gene that maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4 % of the human genome and encodes nearly 900 genes. Thought 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.
- ID gène
- 158055
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