Cell Biology Antibodies 3
Occludin Rabbit Polyclonal Antibody (CAB12621)
- SKU:
- CAB12621
- Product Type:
- Antibody
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Cell Biology
- Reactivity:
- Human, Mouse, Rat
- Synonyms:
- BLCPMG, PTORCH1, PPP1R115, Occludin
- Research Use:
- Cell Biology
Description
Occludin Antibody (CAB12621)
The Occludin Antibody (CAB12621) is a high-quality antibody developed for reliable detection and analysis of target proteins. This antibody, generated in rabbits, exhibits high reactivity with human samples and has been validated for use in Western blot applications. By targeting the occludin protein, this antibody enables researchers to detect and analyze the expression levels of occludin in various cell types, making it ideal for studies related to cell junctions, barrier function, and epithelial/endothelial cell biology.Occludin is a crucial component of tight junctions, which play a pivotal role in regulating paracellular permeability and maintaining tissue integrity.
This antibody is validated for use in WB, ELISA applications and has demonstrated reactivity against Human, Mouse, Rat samples.
| Product Name: | Occludin Antibody |
| SKU: | CAB12621 |
| Size: | 20μL, 100μL |
| Reactivity: | Human, Mouse, Rat |
| Conjugate: | Unconjugated |
| Immunogen: | Recombinant protein (or fragment).This information is considered to be commercially sensitive. | ||||
| Sequence: | VVQE LPLT SPVD DFRQ PRYS SGGN FETP SKRA PAKG RAGR SKRT EQDH YETD YTTG GESC DELE EDWI REYP PITS DQQR QLYK RNFD TGLQ EYKS LQSE L | ||||
| Tested Applications: | WB ELISA | ||||
| Recommended Dilution: |
| ||||
| Synonyms: | BLCPMG, PTORCH1, PPP1R115, Occludin |
| Positive Sample: | 293T |
| Cellular Localization: | Cell Junction, Membrane, Multi-Pass Membrane Protein, Tight Junction. |
| Calculated MW: | 59kDa |
| Observed MW: | 62kDa |
This gene encodes an integral membrane protein that is required for cytokine-induced regulation of the tight junction paracellular permeability barrier. Mutations in this gene are thought to be a cause of band-like calcification with simplified gyration and polymicrogyria (BLC-PMG), an autosomal recessive neurologic disorder that is also known as pseudo-TORCH syndrome. Alternative splicing results in multiple transcript variants. A related pseudogene is present 1.5 Mb downstream on the q arm of chromosome 5.
| Purification Method | Affinity purification |
| Gene ID | 100506658 |
| RRID | AB_2759466 |
| Buffer Information | Store at -20℃. Avoid freeze / thaw cycles. Buffer: PBS containing 50% glycerol, preserved with proclin300 or sodium azide, pH 7.3. |
 | Western blot analysis of lysates from 293T cells, using Occludin Rabbit pAb (CAB12621) at 1:2000 dilution. Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution. Lysates/proteins: 25μg per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit (AbGn00020). Exposure time: 5s. |
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