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Santa Cruz Biotechnology
human munc13 2 Human Munc13 2, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/result/human munc13 2/product/Santa Cruz Biotechnology Average 91 stars, based on 1 article reviews
human munc13 2 - by Bioz Stars,
2026-05
91/100 stars
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WuXi AppTec
rabbit polyclonal α-munc13-2 antibody ![]() Rabbit Polyclonal α Munc13 2 Antibody, supplied by WuXi AppTec, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/result/rabbit polyclonal α-munc13-2 antibody/product/WuXi AppTec Average 90 stars, based on 1 article reviews
rabbit polyclonal α-munc13-2 antibody - by Bioz Stars,
2026-05
90/100 stars
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CRISPR/Cas9 KO Plasmids consists of Munc13-2-specific 20 nt guide RNA sequences derived from the GeCKO (v2) library. For CRISPR gene knockout, gRNA sequences direct the Cas9 protein to induce a site-specific double strand break (DSB)
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Buy from Supplier |
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Gene Silencers generally consist of pools of three to five target-specific 19-25 nucleotide sequences in length. For independent verification of Munc13-2 gene silencing results, individual duplex components or plasmids are also available upon request. Suitable
|
Buy from Supplier |
|
CRISPR/Cas9 KO Plasmids consists of Munc13-2-specific 20 nt guide RNA sequences derived from the GeCKO (v2) library. For CRISPR gene knockout, gRNA sequences direct the Cas9 protein to induce a site-specific double strand break (DSB)
|
Buy from Supplier |
|
CRISPR/Cas9 KO Plasmids consists of Munc13-2-specific 20 nt guide RNA sequences derived from the GeCKO (v2) library. For CRISPR gene knockout, gRNA sequences direct the Cas9 protein to induce a site-specific double strand break (DSB)
|
Buy from Supplier |
|
Gene Silencers generally consist of pools of three to five target-specific 19-25 nucleotide sequences in length. For independent verification of Munc13-2 gene silencing results, individual duplex components or plasmids are also available upon request.
|
Buy from Supplier |
|
CRISPR/Cas9 KO Plasmids consists of Munc13-2-specific 20 nt guide RNA sequences derived from the GeCKO (v2) library. For CRISPR gene knockout, gRNA sequences direct the Cas9 protein to induce a site-specific double strand break (DSB)
|
Buy from Supplier |
|
CRISPR/Cas9 KO Plasmids consists of Munc13-2-specific 20 nt guide RNA sequences derived from the GeCKO (v2) library. For CRISPR gene knockout, gRNA sequences direct the Cas9 protein to induce a site-specific double strand break (DSB)
|
Buy from Supplier |
|
Gene Silencers generally consist of pools of three to five target-specific 19-25 nucleotide sequences in length. For independent verification of Munc13-2 gene silencing results, individual duplex components or plasmids are also available upon request. Suitable
|
Buy from Supplier |
|
Gene Silencers generally consist of pools of three to five target-specific 19-25 nucleotide sequences in length. For independent verification of Munc13-2 gene silencing results, individual duplex components or plasmids are also available upon request.
|
Buy from Supplier |
|
Gene Silencers generally consist of pools of three to five target-specific 19-25 nucleotide sequences in length. For independent verification of Munc13-2 gene silencing results, individual duplex components or plasmids are also available upon request.
|
Buy from Supplier |
Image Search Results
Journal: Proceedings of the National Academy of Sciences of the United States of America
Article Title: Size-dependent mechanism of cargo sorting during lysosome-phagosome fusion is controlled by Rab34
doi: 10.1073/pnas.1206811109
Figure Lengend Snippet: Role of Munc13-2 in the Rab34-dependent regulation of phago-lysosome fusion, (A) Quantitative analysis of EGFP-Munc13-2 association to phagosomes under the different conditions. Data show mean ± SD from one representative experiment out of two with at least 50 cells analyzed in each. (B) Quantitative analysis of endogenous Munc13-2 association to phagosomes in macrophages expressing the indicated constructs. Data show mean ± SD from one representative experiment in which at least 50 cells were analyzed. (C) Association of LAMP-1 to phagosomes in Munc13-2 WT and KO mouse bone marrow–derived macrophages (BMMs). (Right) Quantitative analysis of LAMP-1 fluorescence intensity association to bead phagosomes. (D) Delivery of Dex70kDa to phagosomes in BMMs preloaded with Dex70kD. (Right) Quantitative analysis of Dex70kDa delivery to phagosomes. Mean ± SD from three experiments; at least 100 cells were analyzed. *P ≤ 0.01, **P ≤ 0.001, from two-tailed Student t test. (Scale bar, 10 µm.) (Inset magnification: ∼1.75×.)
Article Snippet:
Techniques: Expressing, Construct, Derivative Assay, Fluorescence, Two Tailed Test