C9ORF173 antibody (AA 201-300) (Biotin)
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- Target See all C9ORF173 products
- C9ORF173 (Chromosome 9 Open Reading Frame 173 (C9ORF173))
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Binding Specificity
- AA 201-300
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Reactivity
- Mouse
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This C9ORF173 antibody is conjugated to Biotin
- Application
- Western Blotting (WB), ELISA
- Cross-Reactivity
- Mouse
- Predicted Reactivity
- Human,Rat,Dog
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C9orf173
- Isotype
- IgG
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- Application Notes
- WB 1:300-5000
- 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.
- Preservative
- ProClin
- Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C for 12 months.
- Expiry Date
- 12 months
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- Target
- C9ORF173 (Chromosome 9 Open Reading Frame 173 (C9ORF173))
- Alternative Name
- C9orf173 (C9ORF173 Products)
- Synonyms
- sperm-tail PG-rich repeat containing 3 antibody, STPG3 antibody
- Background
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Synonyms: C9orf173, Chromosome 9 open reading frame 173, CI173_HUMAN, Uncharacterized protein C9orf173.
Background: C9orf173 (chromosome 9 open reading frame 173) is a 389 amino acid protein that exists as four alternatively spliced isoforms. The gene encoding C9orf173 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.
- Gene ID
- 441476
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