Rabbit Polyclonal S tag antibody. Suitable for ICC/IF and reacts with Tag samples.
pH: 7.2
Preservative: 0.09% Sodium azide
Constituents: 99% PBS
ICC/IF | |
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Tag | Tested |
Species | Dilution info | Notes |
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Species Tag | Dilution info 1/4000 | Notes - |
KETAAAKFERQHMDS tag antibody, S peptide, S peptide epitope tag
Rabbit Polyclonal S tag antibody. Suitable for ICC/IF and reacts with Tag samples.
pH: 7.2
Preservative: 0.09% Sodium azide
Constituents: 99% PBS
Rabbits were immunized with highly purified S-tag peptide conjugated with KLHA and the resulting antiserum was collected and immunoaffinity purified off a peptide immunosorbent.
The S tag is a peptide sequence derived from ribonuclease A commonly used in molecular biology for protein purification and detection. This tag has a molecular mass of approximately 2 kDa. Researchers often utilize S tags for their small size which minimizes interference with protein function. The S tag is typically expressed as a fusion with the protein of interest which enables it to be used as a versatile tool in a variety of expression systems.
S tags do not independently participate in cellular functions but instead facilitate experimental procedures. When fused to a protein the S tag allows for simple detection and purification using anti-S tag antibodies. This functionality makes it possible to isolate and study the protein of interest without affecting its native activity significantly. While S tags do not form part of any specific complex they interact with complexes like alkaline phosphatase in experimental applications to enhance detection signals.
S tags themselves do not have inherent roles in cellular pathways. However they are used as a tool in studies involving signal transduction or metabolic pathways where their presence aids in tracking or manipulating pathway components. Due to their utility S tags can be connected indirectly to proteins such as ALP (alkaline phosphatase) by enabling pathway mapping in experiments.
S tags do not directly relate to specific conditions but are instrumental in research. For instance they allow scientists to study proteins connected to cancer or metabolic disorders more effectively. In research related to metabolic disorders S-tagged proteins can be linked to alkaline phosphatase helping in investigations to understand the role of alkaline phosphatase in calcium metabolism issues.
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Immunofluorescent analysis of 4% paraformaldehyde (PFA) - fixed, permeabilized with 0.1% Triton-X-100 in CHO cells transfected with 12-tags constructs (named as CHO-12 tags) labelling S Tag with ab307272 at 1/4000 dilution (0.25ug/ml), followed by a Donkey Anti-Rabbit IgG (H&L), FITC conjugated secondary antibody at 1/2000 dilution (0.5 ug/ml) (Green). Nucleus was counterstained with DAPI (Blue). Bottom panel images show parallel staining in parental CHO cell line.
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