Products: Primary Antibodies
Anti-Doublecortin Antibody
from Aves Labs
Two antipeptide antibodies were generated in chickens against sequences shared between the mouse (AAT58219.1), rat (NP_445831.3) and human (CAA06617.1) gene products. These antibodies were affinity-purified and then mixed in equal concentrations. These antibodies have been validated with human, mouse and rat tissues.
PRODUCT OPTIONS
| Brand | Catalog # | Option | Volume | Concentration | Price | |
|---|---|---|---|---|---|---|
| Brand |
Catalog # DCX |
Volume 1000 µL |
Concentration 200 µg/mL |
Price $410.00 |
Validation Images
![Doublecortin (DCX, Aves Labs, 1:1000 dilution) staining (GREEN) of a tissue section (4% paraformaldehyde-fixed, paraffin-embedded) through the cochlear ganglion from a neonatal mouse. RED staining is neurofilament [NF-M, Rockland Labs, visualized with Texas Red-goat anti-rabbit IgG (Jackson Immunoresearch)]](http://cdn.shopify.com/s/files/1/0014/8806/0475/products/validation-image-dcx-if-2.jpg?v=1550957188)
![Doublecortin (DCX, Aves Labs, 1:1000 dilution) staining (GREEN) of a tissue section (4% paraformaldehyde-fixed, paraffin-embedded) through the cerebellar cortex of a neonatal mouse. REF staining is neurofilament [NF-M, Rockland Labs, visualized with Texas Red-goat anti-rabbit IgG (Jackson Immunoresearch)]](http://cdn.shopify.com/s/files/1/0014/8806/0475/products/validation-image-dcx-if-3.jpg?v=1550957188)
![Doublecortin (DCX, Aves Labs, 1:1000 dilution) staining (GREEN) of a tissue section (4% paraformaldehyde-fixed, paraffin-embedded) through the cerebellar cortex of a neonatal mouse. RED staining is neurofilament [NF-M, Rockland Labs, visualized with Texas Red-goat anti-rabbit IgG (Jackson Immunoresearch)]](http://cdn.shopify.com/s/files/1/0014/8806/0475/products/validation-image-dcx-if-4.jpg?v=1550957198)
![Doublecortin (DCX, Aves Labs, 1:1000 dilution) staining (RED) of a tissue section (4% paraformaldehyde-fixed, paraffin-embedded) through the cerebral cortical periventricular zone cerebellar cortex of a neonatal mouse. Green staining is neurofilament [NF-M, Rockland Labs, visualized with fluorescein-goat anti-rabbit IgG (Jackson Immunoresearch)]](http://cdn.shopify.com/s/files/1/0014/8806/0475/products/validation-image-dcx-if-5.jpg?v=1550957206)
Product Details
Polyclonal
Chicken
Human Mouse Rat
ICC IHC
Doublecortin is a microtubule-associated protein found in neuroblasts and immature neurons, especially those undergoing embryonic migrations. It was first identified as the X-chromosome-encoded gene product mutated in the human diseases Lissencephaly (in males) and Periventricular Heterotopia (in females), diseases caused by failure of neocortical neuroblast migration. The human protein itself is 360 amino acids (40,044 daltons) and contains doublecortin motifs near its N-terminus that are believed to mediate the microtubule binding.
Chickens were immunized with two synthetic peptide / keyhole limpet hemocyanin (KLH) conjugates. These synthetic peptides corresponded to different regions of the doublecortin gene product, but are shared between the human (CAA06617.1, NCBI) and mouse (AAT58219.1, NCBI) sequences. After repeated injections, immune eggs were collected, and the IgY fractions were purified from the yolks. These IgY fractions were then affinity-purified using a peptide column, and the concentrations of the eluates adjusted to 200 ug/ml. Finally, equal volumes of these affinity-purified antipeptide antibodies were mixed, and the preparation was filter-sterilized.
Neuronal migration protein doublecortin (Doublin) (Lissencephalin-X) (Lis-X)
DCX DBCN LISX
AB_2313540
Antibody Validation and Application Notes
This antibody has been validated using the following assays:
1:1000-1:2000
Quality Control
The following quality control assay is performed on each new lot of this antibody to ensure it meets designated performance requirements.
This anti-peptide antibody mixture was analyzed by immunohistochemistry (at a dilution of 1:2000) using fluorescein-labeled goat anti-chicken IgY (1:500 dilution, Aves Labs Cat.# F-1005) as the secondary reagent.
Citations and References
- Smagin DA, Park JH, Michurina TV, Peunova N, Glass Z, Sayed K, Bondar NP, Kovalenko IN, Kudryavtseva NN, Enikolopov G (2015), 'Altered Hippocampal Neurogenesis and Amygdalar Neuronal Activity in Adult Mice with Repeated Experience of Aggression.' Frontiers in Neurosciene. 10.3389/fnins.2015.00443.
- Lim RG, Salazar LL, Wilton DK, King AR, Stocksdale JT, Sharifabad D, Lau AL, Stevens B, Reidling JC, Winokur ST, Casale MS, Thompson LM, Pardo M, Díaz-Barriga AGG, Straccia M, Sanders P, Alberch J, Canals JM, Kaye JA, Dunlap M, Jo L, May H, Mount E, Anderson-Bergman C, Haston K, Finkbeiner S, Kedaigle AJ, Gipson TA, Yildirim F, Ng CW, Milani P, Housman DE, Fraenkel E, Allen ND, Kemp PJ, Atwal RS, Biagioli M, Gusella JF, MacDonald ME, Akimov SS, Arbez N, Stewart J, Ross CA, Mattis VB, Tom CM, Ornelas L, Sahabian A, Lenaeus L, Mandefro B, Sareen D, Svendsen CN (2017), 'Developmental alterations in Huntington's disease neural cells and pharmacological rescue in cells and mice.' Nature Neuroscience. 10.1038/nn.4532.
- Mellios N, Feldman DA, Sheridan SD, Ip JPK, Kwok S, Amoah SK, Rosen B, Rodriguez BA, Crawford B, Swaminathan R, Chou S, Li Y, Ziats M, Ernst C, Jaenisch R, Haggarty SJ, Sur M (2017), 'MeCP2-regulated miRNAs control early human neurogenesis through differential effects on ERK and AKT signaling.' Molecular Psychiatry. 10.1038/mp.2017.86.
- Mehta SR, Tom CM, Wang Y, Bresee C, Rushton D, Mathkar PP, Tang J, Mattis VB (2018), 'Human Huntington’s Disease iPSC-Derived Cortical Neurons Display Altered Transcriptomics, Morphology, and Maturation.' Cell Reports. 10.1016/j.celrep.2018.09.076.
- A Alachkar, L Wang, R Yoshimura, AR Hamzeh, Z Wang, N Sanathara, SM Lee, X Xu, GW Abbott, and O Civelli (2017), 'Prenatal one-carbon metabolism dysregulation programs schizophrenia-like deficits.' Molecular Psychiatry. 10.1038/mp.2017.164.