C9orf64 antibody (AA 161-260) (Biotin)
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- Target See all C9orf64 products
- C9orf64 (Chromosome 9 Open Reading Frame 64 (C9orf64))
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Binding Specificity
- AA 161-260
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This C9orf64 antibody is conjugated to Biotin
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Application
- Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Cross-Reactivity
- Human
- Predicted Reactivity
- Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C9orf64
- Isotype
- IgG
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- Application Notes
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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.
- 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
- C9orf64 (Chromosome 9 Open Reading Frame 64 (C9orf64))
- Alternative Name
- C9orf64 (C9orf64 Products)
- Synonyms
- C9orf64 antibody, MGC84745 antibody, MGC97544 antibody, chromosome Z C9orf64 homolog antibody, chromosome 9 open reading frame 64 L homeolog antibody, chromosome 9 open reading frame 64 antibody, chromosome 15 open reading frame, human C9orf64 antibody, queuosine salvage protein antibody, CZH9orf64 antibody, c9orf64.L antibody, c9orf64 antibody, C15H9orf64 antibody, C8H9orf64 antibody, C9orf64 antibody
- Background
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Synonyms: C9orf64, CI064_HUMAN, UPF0553 protein C9orf64.
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 C9orf64 gene product has been provisionally designated C9orf64 pending further characterization.
- Gene ID
- 84267
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