Rabbit Polyclonal ZNF316 antibody. Suitable for IP, WB and reacts with Human samples. Immunogen corresponding to Synthetic Peptide within Human ZNF316 aa 450-550.
pH: 6.8 - 7.4
Preservative: 0.09% Sodium azide
Constituents: 99% Tris buffered saline, 0.1% BSA
IP | WB | |
---|---|---|
Human | Tested | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 2-10 µg/mg of lysate | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Zinc finger protein 316, ZNF316
Rabbit Polyclonal ZNF316 antibody. Suitable for IP, WB and reacts with Human samples. Immunogen corresponding to Synthetic Peptide within Human ZNF316 aa 450-550.
pH: 6.8 - 7.4
Preservative: 0.09% Sodium azide
Constituents: 99% Tris buffered saline, 0.1% BSA
ab176708 was affinity purified using an epitope specific to ZNF316 immobilized on solid support.
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ZNF316 also known as Zinc Finger Protein 316 acts as a transcription factor involved in regulating gene expression. It possesses multiple C2H2-type zinc fingers that allow it to bind specifically to DNA sequences influencing transcriptional activity. The protein has an approximate mass of 70 kDa based on sequence data analysis. ZNF316 is expressed in various tissues with notable expression in the brain and reproductive organs suggesting its role in diverse physiological processes.
Zinc finger proteins like ZNF316 contribute to protein-DNA interactions that regulate gene transcription. This protein may interact with other transcriptional regulators to modulate gene expression patterns essential for cell differentiation and development. While ZNF316 has not been documented as part of a well-characterized multi-protein complex its zinc finger domains suggest a potential for forming interactions with co-regulatory proteins or elements influencing chromatin structure.
ZNF316 has a role in the transcriptional regulation within pathways related to neural development and reproductive function. Specifically it appears involved in pathways with genes that are critical for signaling in neural tissue and may interact functionally within the Wnt signaling cascade. This interaction can link it to proteins such as β-catenin although further research may clarify additional pathway-specific interactions.
Scientific studies suggest a relationship between ZNF316 and neurological conditions such as schizophrenia. Aberrations in the expression or function of ZNF316 may contribute to pathogenesis potentially due to disrupted gene regulatory mechanisms in the brain. Furthermore gastrointestinal cancers have been linked to dysregulation in ZNF316 expression or activity possibly involving its interaction with tumor suppressor proteins like p53 therefore affecting cell proliferation and apoptosis. Continued research is necessary to elucidate these associations in greater detail.
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All lanes: Western blot - Anti-ZNF316 antibody (ab176708) at 0.04 µg/mL
Lane 1: HeLa whole cell lysate at 50 µg
Lane 2: HeLa whole cell lysate at 15 µg
Lane 3: Jurkat whole cell lysate at 50 µg
Lane 4: 293T whole cell lysate at 50 µg
Developed using the ECL technique.
Predicted band size: 108 kDa
Exposure time: 30s
ab176708 at 0.4 μg/ml detecting ZNF316 in HeLa whole cell lysate by WB following IP.
Lane 1: ab176708 at 6 μg/mg of lysate
Lane 2: IP with an antibody which recognizes an downstream epitope of ZNF316.
Lane 3: Control IgG.
In each case, 1 mg of lysate was used for IP and 20% of the IP was loaded.
Detection: Chemiluminescence with an exposure time of 3 seconds.
All lanes: Immunoprecipitation - Anti-ZNF316 antibody (ab176708)
Predicted band size: 108 kDa
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