
Anti-GFP Nanobody Agarose Beads KTSM1301
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KTSM 1301 500 μl
Article No.: KTSM1301
Specification: 500 µ l (20 times, 50% nanobody coated Agarose suspension)
Storage condition: 4 ℃ (frozen storage prohibited)
Shelf life: 12 months
Anti-GFP Nanobody Agarose Beads
Anti GFP Agarose Beads are covalently coupled to alpaca anti GFP single domain nano antibodies with high affinity and specificity using agarose beads as a matrix.

Single Domain Antibody (SdAb), also known as Nanobody or VHH (Variable Domain of Heavy Chain), contains only one polypeptide chain, and is the smallest antibody (~15KD) found today that can specifically bind to antigens. The first single domain antibody was intercepted from the variable region of the camel heavy chain antibody (HcAb). Heavy chain antibodies do not have light chains, but consist of only two heavy chains and bind to antigens through a single variable region on the heavy chain. Compared to traditional antibodies, single domain antibodies have multiple advantages, including high affinity (nM-pM), strong specificity, small molecular weight, and can maintain stability under extreme temperature and pH conditions. In addition, single domain antibodies can be produced with high quality and stability, avoiding the issue of batch differences in traditional antibodies.
Green fluorescent protein (GFP) is widely used in protein localization and protein dynamics analysis. Anti GFP Agarose Beads provide rapid and effective one-step immunoprecipitation that can specifically isolate GFP labeled target proteins and their interaction factors from cells and tissues. The isolated products can be used for subsequent biophysical and chemical analysis such as nucleic acid analysis, protein analysis, mass spectrometry analysis, and enzyme biopsy assay.

Suitable for various biochemical reaction analysis:
1. Immunoprecipitation (IP) / Co-IP
2. Mass spectrometry
3. Enzyme activity measurements
4. ChIP / RIP analysis

Advantages of anti mCherry Magarose Beads
Relevant experimental drawings

Reference: Grass car (Ctenopharyngodon idella) GPATCH3 initiates IFN 1 expression via the activation of STING-IRF7 signal axis
The tyrosine kinase SRC of grass carp (Ctenopharyngodon idellus)up-regulates the expression of IFN I by activating TANK binding kinase 1
Specification: 500 µ l (20 times, 50% nanobody coated Agarose suspension)
Storage condition: 4 ℃ (frozen storage prohibited)
Shelf life: 12 months
Anti-GFP Nanobody Agarose Beads
Anti GFP Agarose Beads are covalently coupled to alpaca anti GFP single domain nano antibodies with high affinity and specificity using agarose beads as a matrix.

Single Domain Antibody (SdAb), also known as Nanobody or VHH (Variable Domain of Heavy Chain), contains only one polypeptide chain, and is the smallest antibody (~15KD) found today that can specifically bind to antigens. The first single domain antibody was intercepted from the variable region of the camel heavy chain antibody (HcAb). Heavy chain antibodies do not have light chains, but consist of only two heavy chains and bind to antigens through a single variable region on the heavy chain. Compared to traditional antibodies, single domain antibodies have multiple advantages, including high affinity (nM-pM), strong specificity, small molecular weight, and can maintain stability under extreme temperature and pH conditions. In addition, single domain antibodies can be produced with high quality and stability, avoiding the issue of batch differences in traditional antibodies.
Green fluorescent protein (GFP) is widely used in protein localization and protein dynamics analysis. Anti GFP Agarose Beads provide rapid and effective one-step immunoprecipitation that can specifically isolate GFP labeled target proteins and their interaction factors from cells and tissues. The isolated products can be used for subsequent biophysical and chemical analysis such as nucleic acid analysis, protein analysis, mass spectrometry analysis, and enzyme biopsy assay.

Suitable for various biochemical reaction analysis:
1. Immunoprecipitation (IP) / Co-IP
2. Mass spectrometry
3. Enzyme activity measurements
4. ChIP / RIP analysis

Advantages of anti mCherry Magarose Beads
anti-GFP beads |
Conventional antibody coupled agarose beads |
Direct use | Steps for binding antibodies to protein A/G lipopolysaccharide beads |
No interference from heavy and light chains in downstream applications | Interference from heavy and light chains may occur in downstream applications |
Strict cleaning strips can be used to screen interacting molecules | The optimal conditions for IgG action will limit the use of buffer solutions and have poor tolerance to certain reagents |
Short incubation time (5-30 minutes) | Long incubation time may affect the screening of low affinity interaction factors in CoIP |
Stable quality without batch differences | Batch differences in antibody quality |
Well validated and qualitative | Each antibody requires separate validation |
Generally, the elution product only contains the target protein and its interaction factors, and nano antibodies will not be eluted | In addition to containing target proteins and their interaction factors in the elution product, the antibodies used will also be eluted, and the antibody proteins may affect subsequent detection of target proteins |
Relevant experimental drawings

Reference: Grass car (Ctenopharyngodon idella) GPATCH3 initiates IFN 1 expression via the activation of STING-IRF7 signal axis
The tyrosine kinase SRC of grass carp (Ctenopharyngodon idellus)up-regulates the expression of IFN I by activating TANK binding kinase 1
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