C9orf25 antibody (AA 1-100) (AbBy Fluor® 647)
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- Target See all C9orf25 Antibodies
- C9orf25 (Chromosome 9 Open Reading Frame 25 (C9orf25))
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Binding Specificity
- AA 1-100
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This C9orf25 antibody is conjugated to AbBy Fluor® 647
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Application
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Predicted Reactivity
- Human,Mouse,Rat,Sheep,Horse,Chicken
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C9orf25
- Isotype
- IgG
- Top Product
- Discover our top product C9orf25 Primary Antibody
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- Application Notes
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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.
- 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Expiry Date
- 12 months
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- Target
- C9orf25 (Chromosome 9 Open Reading Frame 25 (C9orf25))
- Alternative Name
- C9orf25 (C9orf25 Products)
- Synonyms
- C9orf25 antibody, bA573M23.5 antibody, C15H9orf25 antibody, 2310028H24Rik antibody, fam219a antibody, zgc:101028 antibody, family with sequence similarity 219 member A antibody, family with sequence similarity 219, member A antibody, family with sequence similarity 219, member Aa antibody, FAM219A antibody, Fam219a antibody, fam219aa antibody
- Background
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Synonyms: bA573M23.5, C9orf25, Chromosome 9 open reading frame 25, F219A_HUMAN, FLJ39031, Hypothetical protein LOC203259, Uncharacterized protein C9orf25.
Background: C9orf25 (chromosome 9 open reading frame 25) is a 185 amino acid protein that exists as seven alternatively spliced isoforms that are encoded by a gene located on human chromosome 9. 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
- 203259
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