CMSS1 antibody (Cy7)
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- Target See all CMSS1 Antibodies
- CMSS1 (Cms Small Ribosomal Subunit 1 (CMSS1))
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Reactivity
- Human, Mouse, Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This CMSS1 antibody is conjugated to Cy7
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Application
- Western Blotting (WB)
- Cross-Reactivity
- Human
- Predicted Reactivity
- Mouse,Rat,Horse
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C3orf26
- Isotype
- IgG
- Top Product
- Discover our top product CMSS1 Primary Antibody
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- Application Notes
- IF(IHC-P) 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
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: 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
- CMSS1 (Cms Small Ribosomal Subunit 1 (CMSS1))
- Alternative Name
- C3orf26 (CMSS1 Products)
- Synonyms
- C3orf26 antibody, 1110001A06Rik antibody, 2610528E23Rik antibody, 4930572F24Rik antibody, AV099812 antibody, AV122629 antibody, RGD1309437 antibody, c3orf26 antibody, C1H3orf26 antibody, cms1 ribosomal small subunit homolog (yeast) antibody, cms small ribosomal subunit 1 antibody, cms1 ribosomal small subunit homolog L homeolog antibody, CMSS1 antibody, Cmss1 antibody, cmss1.L antibody
- Background
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Synonyms: C3orf26, CC026_HUMAN, MGC4308, Uncharacterized protein C3orf26.
Background: Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3. The C3orf26 gene product has been provisionally designated C3orf26 pending further characterization.
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