Purified anti-Pax-6 Antibody (Previously Covance catalog# PRB-278P)

Pricing & Availability
Clone
Poly19013 (See other available formats)
Other Names
Paired box protein Pax-6, oculorhombin, aniridia type II protein, Sey, Protein eyeless, PRB-278P-100
Previously
Covance Catalog# PRB-278P
Isotype
Rabbit Polyclonal IgG
Ave. Rating
Submit a Review
Product Citations
publications
1-Poly19013_PURE_Pax-6_Antibody_1_091420
Whole cell extracts (15µg total protein) from 293T (human), (left panel) or E17 Ms. brain (mouse brain at day 17 of development), (right panel) were resolved by 4-12% Bis-Tris gel electrophoresis, transferred to PVDF membrane and probed with 1.0 µg/mL (1:2000 dilution) of purified Pax-6 rabbit antibody (clone Poly19013) for 2 hr at RT. Proteins were visualized by chemiluminescence detection using HRP Donkey anti-rabbit IgG Antibody (Cat. No. 406401, 1:3000 dilution). Direct-Blot™ HRP anti-GAPDH antibody (Cat. No. 607904) was used as a loading control at 1:25000 dilution (lower). Lane M:Molecular weight marker.
  • 1-Poly19013_PURE_Pax-6_Antibody_1_091420
    Whole cell extracts (15µg total protein) from 293T (human), (left panel) or E17 Ms. brain (mouse brain at day 17 of development), (right panel) were resolved by 4-12% Bis-Tris gel electrophoresis, transferred to PVDF membrane and probed with 1.0 µg/mL (1:2000 dilution) of purified Pax-6 rabbit antibody (clone Poly19013) for 2 hr at RT. Proteins were visualized by chemiluminescence detection using HRP Donkey anti-rabbit IgG Antibody (Cat. No. 406401, 1:3000 dilution). Direct-Blot™ HRP anti-GAPDH antibody (Cat. No. 607904) was used as a loading control at 1:25000 dilution (lower). Lane M:Molecular weight marker.
  • 2-Poly19013_PURE_Pax-6_Antibody_2_091420
    Whole cell extracts (15 µg total protein) from either untransfected 293E cells or transfected with GFP were resolved by 4-12% Bis-Tris gel electrophoresis, transferred to PVDF membrane and probed with 1.0 µg/mL (1:2000 dilution) of purified Pax-6 rabbit antibody (clone Poly19013) (panel A) or purified anti-GFP antibody (clone 1GFP63, Cat. No. 668206) for 2 hr at RT. Proteins were visualized by chemiluminescence detection using HRP Donkey anti-rabbit IgG Antibody (Cat. No. 406401, 1:3000 dilution) or HRP Goat anti-mouse IgG Antibody (Cat. No. 405306, 1:3000 dilution). Direct-Blot™ HRP anti-GAPDH antibody (Cat. No. 607904) was used as a loading control at 1:25000 dilution (lower).Lane M:Molecular weight marker.
  • 3_Purified_Pax-6_Antibody_IHC_2_021315
    IHC staining of purified anti-Pax-6 antibody (clone Poly19013) on formalin-fixed paraffin-embedded mouse brain tissue. Following antigen retrieval using Sodium Citrate H.I.E.R., the tissue was incubated with 20 µg/ml of the primary antibody for 60 minutes at room temperature. BioLegend's Ultra-Streptavidin (USA) HRP kit (Multi-Species, DAB, Cat. No. 929901) was used for detection followed by hematoxylin counterstaining, according to the protocol provided. The image was captured with a 40X objective.
  • 5_Milad_Riazifar
    Frozen human iPSC derived neural rosettes stained with purified anti-Pax-6 (red, clone Poly19013) and ZO-1 (green). Image generously submitted to the 2017 Cell Life Imaging Competition by Milad Riazifar from University of California, Irvine.
Cat # Size Price Quantity Avail. Save
901302 25 µL 92€
Check Availability


Need larger quantities of this item?
Request Bulk Quote
901301 100 µL 281€
Check Availability


Need larger quantities of this item?
Request Bulk Quote
Description

Pax6 is a transcription factor present during embryonic development. The encoded protein contains two different binding sites that are known to bind DNA and function as a regulator of gene transcription. It is a key regulatory gene of eye and brain development. Within the brain, the protein is involved in development of specialized cells that process smell. Pax-6 acts as a critical gene for the development of eyes and other sensory organs, certain neural and epidermal tissues as well as other homologous structures, usually derived from ectodermal tissues. Pax6 serves as a regulator in the coordination and pattern formation required for differentiation and proliferation to successfully take place, ensuring that the processes of neurogenesis and oculogenesis are carried out successfully. As a transcription factor, Pax6 acts at the molecular level in the signaling and formation of the central nervous system. The characteristic paired DNA binding domain of Pax6 utilizes two DNA-binding domains, the paired domain (PD), and the paired-type homeodomain (HD). These domains function separately. An example of this lies in HD’s regulatory involvement in the formation of the lens and retina throughout oculogenesis contrasted by the molecular mechanisms of control exhibited on the patterns of neurogenesis in brain development by PD. The HD and PD domains act in close coordination, giving Pax6 its multifunctional nature in directing molecular signaling in formation of the CNS.

The vertebrate PAX6 locus encodes at least three different protein isoforms, these being the canonical PAX6, PAX6(5a), and PAX6(ΔPD). The canonical PAX6 protein contains an N-terminal paired domain, connected by a linker region to a paired-type homeodomain, and a proline/serine/threonine (P/S/T)-rich C-terminal domain. The paired domain and paired-type homeodomain each have DNA binding activities, while the P/S/T-rich domain possesses a transactivation function. PAX6(5a) is a product of the alternatively spliced exon 5a resulting in a 14 residue insertion in the paired domain which alters the specificity of this DNA binding activity. The nucleotide sequence corresponding to the linker region encodes a set of three alternative translation start codons from which the third PAX6 isoform originates. Collectively known as the PAX6(ΔPD) or pairedless isoforms, these three gene products all lack a paired domain. The pairedless proteins possess molecular weights of 43, 33, or 32kDa, depending on the particular start codon used. PAX6 transactivation function is attributed to the variable length C-terminal P/S/T-rich domain which stretches to 153 residues in human and mouse proteins.

Product Details
Technical Data Sheet (pdf)

Product Details

Reactivity
Human, Mouse, Rat
Antibody Type
Polyclonal
Host Species
Rabbit
Immunogen
This antibody was generated against the peptide (QVPGSEPDMSQYWPRLQ) derived from the C-terminus of the mouse Pax-6 protein.
Formulation
Phosphate-buffered solution + 0.03% Thimerosal.
Preparation
The antibody was purified by affinity chromatography.
Concentration
2 mg/ml
Storage & Handling
The antibody solution should be stored undiluted between 2°C and 8°C. Please note the storage condition for this antibody has been changed from -20°C to between 2°C and 8°C. You can also check your vial or your CoA to find the most accurate storage condition for this antibody.
Application

WB, IHC-P - Quality tested
IF, IHC-F - Reported in the literature, not verified in house

Recommended Usage

Each lot of this antibody is quality control tested by Western blotting and formalin-fixed paraffin-embedded immunohistochemical staining of brain tissue. For Western blotting, the suggested use of this reagent is 1.0 µg/ml (1:2000). For immunohistochemistry, a dilution of 1:50 - 1:100 is suggested. It is recommended that the reagent be titrated for optimal performance for each application.

Application Notes

This antibody weakly reacts with rat. It has also shown reactivity with GFP and is therefore not recommended for use in GFP-expressing systems (as determined by in-house testing).

Pax-6 has two isoforms in human and mice at 46.6 and 48.2 Kd. This antibody recognizes both. The sequence is highly conserved among Pax-6 of various species. The antibody was subsequently purified on a Protein A column and is useful in studying brain, neuronal and olfactory development in higher eukaryotes.

This clone is not recommended for ChIP (Chromatin Immunoprecipitation) assays (as determined by in-house testing).

Application References

(PubMed link indicates BioLegend citation)
  1. Tang K, et al. 2012. Development. 139:1630. (IF) PubMed
  2. Bandah D, et al. 2007. Invest. Ophthalmol. Vis. Sci. 48:2503. (WB) PubMed
  3. Marquardt T, et al. 2001. Cell. 105:43.
  4. Yamamoto Y, Jeffery WR. 2000. Science. 289:631
  5. Ashery-Padan R, et al. 2000. Genes Dev. 14:2701.
  6. Osumi N, et al. 1997. Development. 124:2961.
  7. Koroma BM, et al. 1997. Invest. Ophthalmol Vis Sci. 38:108.
  8. Davis JA, Reed RR. 1996. J Neurosci. 16:5082. (IHC)
  9. Quadrato G, et al. Nature. 545:48. (IF) PubMed
Product Citations
  1. Small K, et al. 2015. Ophthalmology. 13: 681-685. PubMed
  2. Ahmad Z, et al. 2015. PLoS One. 10: 0144597. PubMed
  3. Verheyen A, et al. 2015. PLoS One. 10: 0146127. PubMed
  4. Bandah D, et al. 2007. Invest Ophthalmol Vis Sci. 48:2503-2509. PubMed
  5. Tang K, et al. 2012. Development. 139:1630-1639. PubMed
  6. Delépine C, et al. 2016. Hum Mol Genet. 25: 146 - 157. PubMed
  7. Bando Y, et al. 2016. Cereb Cortex. 26: 106 - 117. PubMed
  8. Pataskar A, et al. 2016. EMBO J. 35: 24 - 45. PubMed
  9. Martínez-Cerdeño V, et al. 2016. Cereb Cortex. 26: 374 - 383. PubMed
  10. Conrad E, et al. 2016. Am J Physiol Endocrinol Metab. 310: E91 - E102. PubMed
  11. Radonjić N, et al. 2016. Cereb Cortex. 26: 131 - 143. PubMed
  12. Taverna E, et al. 2016. Sci Rep. 6:21206. PubMed
  13. Sancho-Martinez I, et al. 2016. Nat Commun. 7:10743. PubMed
  14. Wang W, et al. 2016. Nat Commun. 7:10936. PubMed
  15. Lin H, et al. 2016. Nature. 531:323-328. PubMed
  16. Xu J, et al. 2016. Sci Transl Med. 8: 333ra48. PubMed
  17. Otani T, et al. 2016. Cell Stem Cell. 18: 467-480. PubMed
  18. Paquet D, et al. 2016. Nature. 533: 125-129. PubMed
  19. Okamoto M, et al. 2016. Nat Commun. 7: 11349. PubMed
  20. Wang L, Hou S, Han Y 2016. Nat Neurosci. 19: 888-896. PubMed
  21. Cugola F, et al. 2016. Nature. 534: 267-271. PubMed
  22. Takeo Y, et al. 2016. Sci Rep. 6: 25180. PubMed
  23. He S, et al. 2016. Development. 143: 1937 - 1947. PubMed
  24. Anda F, et al. 2016. Nat Neurosci. 10.1038/nn.4328. PubMed
  25. Moura D, et al. 2016. Sci Rep. 6:28532. PubMed
  26. Plaisted W, et al. 2016. PLoS One. 11: 0157620. PubMed
  27. Toda T, et al. 2016. Sci Rep. 6:29578. PubMed
  28. Abdullah A, et al. 2016. Stem Cell Reports. 7:69-79. PubMed
  29. Feng J, et al. 2016. Cereb Cortex. 26: 3323 - 3334. PubMed
  30. Wiley L, et al. 2016. Sci Rep. 6:30742. PubMed
  31. Bonney S, et al. 2016. J Neurosci. 36: 7786 - 7801. PubMed
  32. Tian E, et al. 2016. Cell Rep. 16: 781-792. PubMed
  33. Hickmott J, et al. 2016. Mol Ther Methods Clin Dev. 3:16051. PubMed
  34. Gey M, et al. 2016. J Neurosci. 36: 9057 - 9069. PubMed
  35. Garreta E, et al. 2016. Biomaterials. 98:64-78. PubMed
  36. Tachibana N, et al. 2016. J Neurosci. 36: 9454 - 9471. PubMed
  37. Broix L, et al. 2016. Nat Genet. 48:1349-1358. PubMed
  38. Pei S, et al. 2016. Sci Rep. 6:33822. PubMed
  39. Zhu L, et al. 2016. J Cell Biol. 215: 187 - 202. PubMed
  40. Simonin Y, et al. 2016. EBioMedicine. 12:161-169. PubMed
  41. M Rodriguez, S Noctor, E Muñoz 2016. PLoS One. 11:e0167063. PubMed
  42. Lajko M, et al. 2016. PLoS One. 11:e0166886. PubMed
  43. Damiani D, et al. 2016. Nat Commun. 7:13509. PubMed
  44. C Tao, X Zhang, 2016. Cell Rep. 17:1832-1844. PubMed
  45. Retallack H, et al. 2016. Proc Natl Acad Sci U S A. 113(50):14408-14413. PubMed
  46. Harkin L, et al. 2016. Cereb Cortex. 10.1093/cercor/bhw394. PubMed
  47. Boland M, et al. 2017. Brain. 10.1093/brain/aww357. PubMed
  48. Breuss M, et al. 2017. Hum Mol Genet. 10.1093/hmg/ddw383. PubMed
  49. Subramanian L, et al. 2017. Nat Commun. 8:14167. PubMed
  50. Lardelli R, et al. 2017. Nat Genet. 10.1038/ng.3762. PubMed
  51. Ren R, et al. 2017. Cell Res. 10.1038/cr.2017.18. PubMed
  52. Miyashita H, et al. 2017. Sci Rep. 7:43557. PubMed
  53. Hayashi R, et al. 2017. Nat Protoc. 10.1038/nprot.2017.007. PubMed
  54. Mills T, et al. 2017. PLoS One.. 10.1371/journal.pone.0176905. PubMed
  55. Sun D, et al. 2017. PLoS One. 12(6):e0179047. PubMed
  56. Zhu Y, et al. 2017. Lab Chip. 10.1039/c7lc00682a. PubMed
  57. Janssens S, et al. 2018. mSystems. 3. PubMed
  58. Shafa M, et al. 2018. Front Med (Lausanne). 9:1816. PubMed
  59. Dhumale P, et al. 2018. PLoS One. 9:1544. PubMed
  60. Chau KF, et al. 2018. Elife. 19:E663. PubMed
  61. Luisier R, et al. 2018. Nat Commun. 8:6458. PubMed
  62. Scior A, et al. 2018. EMBO J. 37:282. PubMed
  63. Ing-Esteves S, et al. 2018. J Neurosci. 38:2713. PubMed
  64. Hickmott JW, et al. 2018. Gene Ther. 25:524. PubMed
  65. Han S, et al. 2018. Development. 145:. PubMed
  66. Lu HC, et al. 2017. Nat Genet. 49:527. PubMed
  67. Andres LM, et al. 2017. ACS Chem Biol. 12:2030. PubMed
  68. Hoshino A, et al. 2017. Dev Cell. 43:763. PubMed
  69. Goodson NB, et al. 2018. Dev Biol. 434:149. PubMed
  70. Xu D, et al. 2018. PLoS Biol. 16:e2006613. PubMed
  71. Robson JP, et al. 2019. PLoS One. 14:e0210665. PubMed
  72. Lim Y, et al. 2019. Sci Rep. 9:226. PubMed
  73. Ward JM, et al. 2019. Cell Rep. 26:1189. PubMed
  74. Broix L, et al. 2018. Hum Mol Genet. 27:224. PubMed
  75. Nowakowski TJ, et al. 2018. Nat Neurosci. 21:1784. PubMed
  76. Ren X, et al. 2019. Cell Rep. 26:3643. PubMed
  77. Langer LF, et al. 2019. Elife. 8. PubMed
  78. Todd L, et al. 2017. Glia. 65:1640. PubMed
  79. Remez LA, et al. 2017. Dev Biol. 432:140. PubMed
  80. Bovio PP, et al. 2019. Mol Neurobiol. 56:4273. PubMed
  81. Wilson CS, et al. 2019. JCI Insight. 5. PubMed
  82. Zurkirchen L, et al. 2019. Nat Commun. 10:2192. PubMed
  83. Wang H, et al. 2019. Cell Rep. 27:2335. PubMed
  84. Palencia–Campos A, et al. 2017. Hum Mol Genet. 26:4556. PubMed
  85. Jin J, et al. 2019. PLoS One. 14:e0219362. PubMed
  86. Dominguez Gonzalez B, et al. 2018. Hum Mol Genet. 27:2154. PubMed
  87. Nazir FH, et al. 2018. Neurochem Int. 121:38. PubMed
  88. Docampo–Seara A, et al. 2019. Brain Struct Funct. 224:2325. PubMed
  89. Wang S, et al. 2019. Protein Cell. 10:1. PubMed
  90. Kawaue T, et al. 2019. Nat Commun. 10:2780. PubMed
  91. Karzbrun E, et al. 2018. Nat Phys. 14:515. PubMed
  92. Segarra M, et al. 2018. Science. 361:eaao2861. PubMed
  93. Ooi J, et al. 2019. Cell Rep. 26:2494. PubMed
  94. Liu Z, et al. 2019. Cell Rep. 27:3832. PubMed
  95. Bashford AL, et al. 2019. J Pathol. 248:396. PubMed
  96. Hu XL, et al. 2017. Neuron. 95:309. PubMed
  97. Todd L, et al. 2018. Stem Cells. 36:392. PubMed
  98. Wang Q, et al. 2017. Curr Biol. 27:1791. PubMed
  99. Docampo–Seara A, et al. 2018. Brain Struct Funct. 223:3593. PubMed
  100. Mochizuki T, et al. 2017. Development. 144:708. PubMed
  101. Zhang X, et al. 2019. Protein Cell. 10:649. PubMed
  102. Watanabe Y, et al. 2018. Development. 145. PubMed
  103. Kurabayashi N, et al. 2018. Development. 145. PubMed
  104. Postel M, et al. 2019. BMC Bioinformatics. 20:470. PubMed
  105. Sanchez–Guardado L, et al. 2019. Elife. 8:e46675. PubMed
  106. Peter CJ, et al. 2019. Nat Commun. 10:4112. PubMed
  107. Tu J et al. 2018. Stem cell research. 28:29-32 . PubMed
  108. Shibata S et al. 2018. Cell reports. 25(6):1668-1679 . PubMed
  109. Zhang Y et al. 2018. Cell stem cell. 23(4):516-529 . PubMed
  110. Zahr SK et al. 2018. Neuron. 97(3):520-537 . PubMed
  111. Nakano Y et al. 2018. Cell. 174(3):536-548 . PubMed
  112. Thomas Klein et al. 2018. Stem cell research. 33:171-174 . PubMed
  113. Baizabal JM et al. 2018. Neuron. 98(5):945-962 . PubMed
  114. Thomas Klein et al. 2018. Stem cell research. 31:222-226 . PubMed
  115. Tang Y et al. 2018. Cell reports. 24(5):1355-1362 . PubMed
  116. Diacou R et al. 2018. Cell reports. 25(9):2510-2523 . PubMed
  117. Alexander JM et al. 2019. Elife. 8 pii: e41769. PubMed
  118. Roy A et al. 2019. Elife. 8 pii: e45961. PubMed
  119. Ibañez Rodriguez MP et al. 2018. The Journal of comparative neurology. 526(15):2462-2481 . PubMed
  120. Del Toro D et al. 2017. Cell. 169(4):621-635 . PubMed
  121. Liu J et al. 2017. Cell stem cell. 21(5):635-649 . PubMed
  122. Klein T et al. 2019. Stem cell research. 1724:56:00 . PubMed
  123. Gao F et al. 2019. Mol Cell. 75(5):891-904 . PubMed
  124. Alzu'bi A et al. 2019. Journal of anatomy. 235(3):555-568 . PubMed
  125. Lavado A et al. 2018. Dev Cell. 47(5):576-591 . PubMed
  126. Homman‐Ludiye J et al. 2018. The Journal of comparative neurology. 526(17):2870-2883 . PubMed
  127. Cliff TS et al. 2017. Cell stem cell. 21(4):502-516 . PubMed
  128. Beattie R et al. 2017. Neuron. 94(3):517-533 . PubMed
  129. Gabriel E et al. 2017. Cell stem cell. 20(3):397-406 . PubMed
  130. Sano N et al. 2017. Frontiers in cellular neuroscience. 0.54375 . PubMed
  131. Kim YJ, et al. 2018. Neuron. 100:1180. PubMed
  132. Le Dréau G, et al. 2018. Elife. 7:e7267. PubMed
  133. Cargnin F, et al. 2018. Neuron. 100:1083. PubMed
  134. Uzquiano A, et al. 2019. Cell Rep. 28:1596. PubMed
  135. Forrest MP, et al. 2017. Cell Stem Cell. 1.086805556. PubMed
  136. Parween S, et al. 2018. Front Cell Neurosci. 0.746527778. PubMed
  137. Miesfeld JB, et al. 2018. Sci Rep. 8:10195. PubMed
  138. Chen Y, et al. 2019. Methods Mol Biol. 1919:59:00. PubMed
  139. Velasco S, et al. 2019. Nature. 570:523. PubMed
  140. Moore D, et al. 2019. Stem Cells Int. 2019:8710180. PubMed
  141. Bonnefont J, et al. 2019. Neuron. 103:1096. PubMed
  142. Wörsdörfer P, et al. 2019. Sci Rep. 9:15663. PubMed
  143. Panagiotakos G, et al. 2019. Elife. 8:e51037. PubMed
  144. Pandey PR, et al. 2019. Int J Mol Sci. 0.936805556. PubMed
  145. Shafa M, et al. 2019. Int J Mol Sci. 0.95. PubMed
  146. Laan L, et al. 2020. Clin Epigenetics. 12:09. PubMed
  147. Wu X, et al. 2018. Cell. 172:423. PubMed
  148. Tripathy R, et al. 2018. Neuron. 100:1354. PubMed
  149. Chang CH, et al. 2019. Dev Cell. 48:184. PubMed
  150. Wu Z, et al. 2019. Neuron. 101:635. PubMed
  151. Pollen AA, et al. 2019. Cell. 176:743. PubMed
  152. Matsumura K, et al. 2020. Nat Commun. 11:859. PubMed
  153. Plaza Reyes A, et al. 2020. Nat Commun. 11:1609. PubMed
  154. Fregeac J, et al. 2020. Mol Autism. 11:22. PubMed
  155. Popovitchenko T, et al. 2020. Nat Commun. 11:1674. PubMed
  156. Mirjalili Mohanna SZ, et al. 2020. Mol Ther Methods Clin Dev. 17:478. PubMed
  157. Lindsay CD, et al. 2019. Acta Biomater. 95:225. PubMed
  158. Mao X, et al. 2019. Stem Cell Reports. 13:747. PubMed
  159. Saito K, et al. 2019. Cell Rep. 29:1555. PubMed
  160. Komabayashi-Suzuki M, et al. 2019. Cell Rep. 29:1113. PubMed
  161. Li L, et al. 2019. Cell Rep. 28:698. PubMed
  162. Yin WC, et al. 2019. Dev Cell. 48:167. PubMed
  163. Gao ML, et al. 2020. Front Cell Dev Biol. 8:128. PubMed
  164. Bershteyn M, et al. 2017. Cell Stem Cell. 20:435. PubMed
  165. Shu P, et al. 2019. J Biol Chem. 294:3444. PubMed
  166. Ding W, et al. 2019. J Neurosci. 39:1994. PubMed
  167. Ramzy A, et al. 2018. Endocrinology. 159:83. PubMed
  168. Omer Javed A, et al. 2018. Cell Rep. 25:368. PubMed
  169. Cheng S, et al. 2019. J Neurosci. 39:2195. PubMed
RRID
AB_2749901 (BioLegend Cat. No. 901302)
AB_2565003 (BioLegend Cat. No. 901301)

Antigen Details

Cell Type
Neural Stem Cells
Biology Area
Cell Biology, Neuroscience, Neuroscience Cell Markers, Signal Transduction, Stem Cells, Synaptic Biology, Transcription Factors
Molecular Family
Nuclear Markers
Gene ID
5080 View all products for this Gene ID 18508 View all products for this Gene ID 25509 View all products for this Gene ID
UniProt
View information about Pax-6 on UniProt.org

Related FAQs

There are no FAQs for this product.
Go To Top Version: 7    Revision Date: 09.04.2020

For research use only. Not for diagnostic use. Not for resale. BioLegend will not be held responsible for patent infringement or other violations that may occur with the use of our products.

 

*These products may be covered by one or more Limited Use Label Licenses (see the BioLegend Catalog or our website, www.biolegend.com/ordering#license). BioLegend products may not be transferred to third parties, resold, modified for resale, or used to manufacture commercial products, reverse engineer functionally similar materials, or to provide a service to third parties without written approval of BioLegend. By use of these products you accept the terms and conditions of all applicable Limited Use Label Licenses. Unless otherwise indicated, these products are for research use only and are not intended for human or animal diagnostic, therapeutic or commercial use.

 

BioLegend Inc., 8999 BioLegend Way, San Diego, CA 92121 www.biolegend.com
Toll-Free Phone: 1-877-Bio-Legend (246-5343) Phone: (858) 768-5800 Fax: (877) 455-9587

This data display is provided for general comparisons between formats.
Your actual data may vary due to variations in samples, target cells, instruments and their settings, staining conditions, and other factors.
If you need assistance with selecting the best format contact our expert technical support team.

ProductsHere
Insert Note Here
Save Close Clear
Lab Timer
Tools
Login / Register
Forgot your password? Reset password?
Create an Account