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Alexa Fluor® 488 anti-human CD326 (EpCAM) Anti
产品名称:
Alexa Fluor® 488 anti-human CD326 (EpCAM) Anti
产品类别:
抗体
产品编号:
324209
产品应用:
324209
[价格]
规格 价格 库存
25tests ¥ 1692 1

产品详情

Product Details

Verified Reactivity
Human
Antibody Type
Monoclonal
Host Species
Mouse
Immunogen
DU.4475 breast carcinoma
Formulation
Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide and BSA (origin USA)
Preparation
The antibody was purified by affinity chromatography and conjugated with Alexa Fluor? 488 under optimal conditions.
Concentration
Lot-specific (to obtain lot-specific concentration, please enter the lot number in our Concentration and Expiration Lookup or Certificate of Analysis online tools.)
Storage & Handling
The antibody solution should be stored undiluted between 2°C and 8°C, and protected from prolonged exposure to light. Do not freeze.
Application

FC - Quality tested
SB -?Reported in the literature, not verified in house

Recommended Usage

Each lot of this antibody is quality control tested by immunofluorescent staining with flow cytometric analysis. For flow cytometric staining, the suggested use of this reagent is 5 ?L per million cells in 100 ?L staining volume or 5 ?L per 100 ?L of whole blood. It is recommended that the reagent be titrated for optimal performance for each application.

* Alexa Fluor? 488 has a maximum emission of 519 nm when it is excited at 488 nm.


Alexa Fluor? and Pacific Blue? are trademarks of Life Technologies Corporation.

View full statement regarding label licenses
Excitation Laser
Blue Laser (488 nm)
Application Notes

Additional reported applications (for the revelant formats) include: immunofluorescence,?immunohistochemistry3, and spatial biology (IBEX)4,5.

Additional Product Notes

Iterative Bleaching Extended multi-pleXity (IBEX) is a fluorescent imaging technique capable of highly-multiplexed spatial analysis. The method relies on cyclical bleaching of panels of fluorescent antibodies in order to image and analyze many markers over multiple cycles of staining, imaging, and, bleaching. It is a community-developed open-access method developed by the Center for Advanced Tissue Imaging (CAT-I) in the National Institute of Allergy and Infectious Diseases (NIAID, NIH).

Application References

(PubMed link indicates BioLegend citation)
  1. Lammers R, et al. 2002. Exp. Hematol. 30:537.
  2. Schultz LD, et al. 2010. P. Natl. Acad. Sci. USA 107:13022. PubMed
  3. Human Protein Atlas http://www.proteinatlas.org/ENSG00000119888/antibody (IHC)
  4. Radtke AJ,?et al. 2020.?Proc Natl Acad Sci USA. 117:33455-33465. (SB)?PubMed
  5. Radtke AJ,?et al. 2022.?Nat Protoc. 17:378-401. (SB)?PubMed
Product Citations
  1. Zabala M, et al. 2020. Cell Stem Cell. 27(2):284-299.e8. PubMed
  2. Carraro G, et al. 2021. Nat Med. 27:806. PubMed
  3. Yu L, et al. 2020. Cell Stem Cell. 28(3):550-567.e12. PubMed
  4. Howden SE, et al. 2020. Cell Stem Cell. 28(4):671-684.e6. PubMed
  5. Palkowitz AL, et al. 2021. Adv Healthc Mater. 10:e2100132. PubMed
  6. Pal D et al. 2017. eLife. 6 pii: e21615. PubMed
  7. Pyo DH, et al. 2020. Cancer Biol Ther. 495:21. PubMed
  8. Morsing M, et al. 2020. Breast Cancer Res. 0.9875. PubMed
  9. Inde Z, et al. 2021. Sci Adv. 7:. PubMed
  10. Sullivan NT, et al. 2022. STAR Protoc. 3:101367. PubMed
  11. Cai X, et al. 2014. PLoS One. 9:108942. PubMed
  12. Calandrini C, et al. 2020. Nat Commun. 11:1310. PubMed
  13. Gerdur ísberg ó, et al. 2019. Sci Rep. 9:14843. PubMed
  14. Safaric Tepes P, et al. 2021. Elife. 10: . PubMed
  15. Hu H et al. 2018. Cell. 175(6):1591-1606 . PubMed
  16. Chen D, et al. 2019. Cell Rep. 29:4568. PubMed
  17. Cardenas JJ, et al. 2020. Methods Enzymol. 415:631. PubMed
  18. Gell JJ, et al. 2018. Stem Cell Res. 27:46. PubMed
  19. Hancock GV, et al. 2021. Stem Cell Res. 55:102493. PubMed
  20. Noort V, et al. 2014. Cancer Res. 74:5690. PubMed
  21. Morris K, et al. 2014. PLoS One. 9:98656. PubMed
  22. Hong HK, et al. 2019. Oncol Rep. 42:2029. PubMed
  23. Chen D et al. 2018. Cell reports. 25(13):3591-3602 . PubMed
  24. Vanslambrouck JM, et al. 2019. J Am Soc Nephrol. 30:1811. PubMed
  25. Staudte S, et al. 2022. Cancers (Basel). 14:. PubMed
  26. Vanslambrouck JM, et al. 2022. Nat Commun. 13:5943. PubMed
  27. Chen D, et al. 2017. Biol Reprod. 97:850. PubMed
  28. Cai X, et al. 2017. Neoplasia. 10.1016/j.neo.2017.03.005. PubMed
  29. Chitiashvili T, et al. 2020. Nat Cell Biol. 22:1436. PubMed
  30. Sandlin CW, et al. 2022. PLoS One. 17:e0274091. PubMed
  31. Pandolfi EC, et al. 2022. Cell Rep Med. 3:100782. PubMed
  32. Koyama M et al. 2019. Immunity. 51(5):885-898 . PubMed
  33. Horwitz K, et al. 2008. Proc Natl Acad Sci U S A. 105:5774. PubMed
  34. Jeong HO, et al. 2022. iScience. 25:105358. PubMed
  35. Mourcin F, et al. 2021. Immunity. . PubMed
  36. Catenacci D, et al. 2015. Gastroenterology. 149: 1794-1803.e4. PubMed
  37. Forbes TA, et al. 2018. Am J Hum Genet. 102:816. PubMed
RRID
AB_756083 (BioLegend Cat. No. 324209) AB_756084 (BioLegend Cat. No. 324210)

Antigen Details

Structure
Type I transmembrane protein, contains six disulfide bridges, one THYRO domain, approximate molecular weight 40 kD.
Distribution

Highly expressed in bone marrow, colon, lung, and most normal epithelial cells. Also highly expressed on carcinomas of gastrointestinal origin. Expressed during early erythrogenesis.

Function
Homotypic calcium-independent cell adhesion. CD326 is believed to be involved in carcinogenesis by its ability to induce genes involved in cellular metabolism and proliferation.
Modification
Glycosylated.
Cell Type
Embryonic Stem Cells, Epithelial cells
Biology Area
Cell Biology, Immunology, Stem Cells
Molecular Family
Adhesion Molecules, CD Molecules
Antigen References

1. Strnad J, et al. 1989. Cancer Res. 49:314.
2. Munz M, et al. 2004. Oncogene 23:5748.
3. Rao CG, et al. 2005. Int. J. Oncol. 27:49.

Gene ID
4072 View all products for this Gene ID
UniProt
View information about CD326 on UniProt.org

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