C9orf68 antibody (AA 201-300) (AbBy Fluor® 750)
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- Target See all C9orf68 products
- C9orf68 (Chromosome 9 Open Reading Frame 68 (C9orf68))
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Binding Specificity
- AA 201-300
- Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This C9orf68 antibody is conjugated to AbBy Fluor® 750
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Application
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Predicted Reactivity
- Human
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C9orf68
- 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
- C9orf68 (Chromosome 9 Open Reading Frame 68 (C9orf68))
- Alternative Name
- C9orf68 (C9orf68 Products)
- Synonyms
- MGC131199 antibody, MGC146453 antibody, C9orf68 antibody, bA6J24.2 antibody, spermatogenesis associated 6-like L homeolog antibody, spermatogenesis associated 6-like antibody, spermatogenesis associated 6 like antibody, spata6l.L antibody, spata6l antibody, SPATA6L antibody
- Background
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Synonyms: bA6J24.2, chromosome 9 open reading frame 68, FLJ10058, RP11-280I16.2, Uncharacterized protein C9orf68,SPA6L_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 C9orf68 gene product has been provisionally designated C9orf68 pending further characterization. There are two isoforms of C9orf68 that are produced as a result of alternative splicing events.
- Gene ID
- 55064
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