MRNIP/C5ORF45 antibody (AA 1-100) (AbBy Fluor® 594)
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- Target See all MRNIP/C5ORF45 (C5ORF45) products
- MRNIP/C5ORF45 (C5ORF45) (Chromosome 5 Open Reading Frame 45 (C5ORF45))
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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 MRNIP/C5ORF45 antibody is conjugated to AbBy Fluor® 594
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Application
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Predicted Reactivity
- Human,Mouse,Rat,Cow,Sheep,Pig,Horse
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C5orf45
- 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
- MRNIP/C5ORF45 (C5ORF45) (Chromosome 5 Open Reading Frame 45 (C5ORF45))
- Alternative Name
- C5orf45 (C5ORF45 Products)
- Synonyms
- 2900016G09Rik antibody, AI851514 antibody, AW475975 antibody, MRN complex interacting protein antibody, zgc:123335 antibody, MRNIP antibody, Mrnip antibody, zgc:123335 antibody
- Background
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Synonyms: Chromosome 5 open reading frame 45, DKFZp686L2452, LOC51149, MGC65027, MGC78537, UPF0544 protein C5orf45, CE045_HUMAN.
Background: C5orf45 is a With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6 % of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf45 gene product has been provisionally designated C5orf45 pending further characterization.
- Gene ID
- 51149
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