CMSS1 antibody (AA 101-200)
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- Target See all CMSS1 Antibodies
- CMSS1 (Cms Small Ribosomal Subunit 1 (CMSS1))
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Binding Specificity
- AA 101-200
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This CMSS1 antibody is un-conjugated
- Application
- Western Blotting (WB), ELISA
- Cross-Reactivity
- Human
- Predicted Reactivity
- Mouse,Rat,Horse
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C3orf26
- Isotype
- IgG
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- Application Notes
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WB 1:300-5000
ELISA 1:500-1000 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- Storage Comment
- Shipped at 4°C. Store at -20°C for one year. 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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