C9orf78 antibody (AA 21-120) (Cy7)
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- Target See all C9orf78 (C9orf98) products
- C9orf78 (C9orf98) (Chromosome 9 Open Reading Frame 78 (C9orf98))
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Binding Specificity
- AA 21-120
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This C9orf78 antibody is conjugated to Cy7
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Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
- Predicted Reactivity
- Human,Mouse,Rat,Dog,Cow,Pig,Horse
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C9orf78
- Isotype
- IgG
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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
- C9orf78 (C9orf98) (Chromosome 9 Open Reading Frame 78 (C9orf98))
- Alternative Name
- C9orf78 (C9orf98 Products)
- Synonyms
- HCA59 antibody, HSPC220 antibody, bA409K20.3 antibody, MGC84248 antibody, MGC186018 antibody, RP23-221O14.10 antibody, chromosome 9 open reading frame 78 antibody, chromosome 17 C9orf78 homolog antibody, chromosome 9 open reading frame 78 L homeolog antibody, zgc:103692 antibody, chromosome 9 C9orf78 homolog antibody, chromosome 11 open reading frame, human C9orf78 antibody, chromosome 9 open reading frame, human C9orf78 antibody, chromosome 17 open reading frame, human C9orf78 antibody, cDNA sequence BC005624 antibody, C9orf78 antibody, C17H9orf78 antibody, c9orf78.L antibody, zgc:103692 antibody, C9H9orf78 antibody, C11H9orf78 antibody, c9orf78 antibody, BC005624 antibody
- Background
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Synonyms: bA409K20.3, C9orf78, Chromosome 9 open reading frame 78, CI078_HUMAN, HCA59, Hepatocellular carcinoma associated antigen 59, Hepatocellular carcinoma-associated antigen 59, HSPC220, Uncharacterized protein C9orf78.
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 C9orf78 gene product has been provisionally designated C9orf78 pending further characterization.
- Gene ID
- 51759
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