C9orf6 antibody (AA 1-100) (HRP)
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- Target See all C9orf6 (FAM206A) Antibodies
- C9orf6 (FAM206A) (Family with Sequence Similarity 206, Member A (FAM206A))
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Binding Specificity
- AA 1-100
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Reactivity
- Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This C9orf6 antibody is conjugated to HRP
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Application
- ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Cross-Reactivity
- Rat
- Predicted Reactivity
- Human,Mouse,Dog,Cow,Sheep,Pig,Horse
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C9orf6
- Isotype
- IgG
- Top Product
- Discover our top product FAM206A Primary Antibody
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- Application Notes
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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.
- Handling Advice
- Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Expiry Date
- 12 months
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- Target
- C9orf6 (FAM206A) (Family with Sequence Similarity 206, Member A (FAM206A))
- Alternative Name
- C9orf6 (FAM206A Products)
- Synonyms
- Fam206a antibody, C9orf6 antibody, CG-8 antibody, C8H9orf6 antibody, C2H9orf6 antibody, si:ch211-254e15.2 antibody, zgc:153072 antibody, family with sequence similarity 206, member A antibody, family with sequence similarity 206 member A antibody, Fam206a antibody, FAM206A antibody, fam206a antibody
- Background
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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.
- Gene ID
- 54942
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