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CKM Antibody
人 VIPR2 / VPAC2 人细胞裂解液 (阳性
鼠抗人绒毛膜促性腺激素单克隆抗体/HC
[VIP第1年] 指数:2
通过海淀分局认证 
CHIP-PCR
1.5M Tris-HCl,pH8.8| 货号： | MAB377 |
| 抗体名： | Anti-NeuN Antibody, clone A60 |
| 抗体英文名： | Anti-NeuN Antibody, clone A60 |
| 应用范围： | FC, ICC, IF, IHC, IH(P), IP, WB |
| 宿主： | Mouse |
| 适应物种： | Avian Chicken Ferret Human Mouse Pig Rat Salamander |
| 克隆性： | 是 |
| 保存条件： | 2-8℃ |
| 免疫原： | Purified cell nuclei from mouse brain |
| 规格： | 500ug |
| Species Reactivity | Key Applications | Host | Format | Antibody Type |
|---|---|---|---|---|
| Av, Ch, Ft, H, M, Po, R, Sal | FC, ICC, IF, IHC, IH(P), IP, WB | M | Purified | Monoclonal Antibody |
| Description | |
|---|---|
| Catalogue Number | MAB377 |
| Brand Family | Chemicon® |
| Trade Name |
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| Description | Anti-NeuN Antibody, clone A60 |
| Alternate Names |
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| Background Information | NeuN antibody (NEUronal Nuclei; clone A60) specifically recognizes the DNA-binding, neuron-specific protein NeuN, which is present in most CNS and PNS neuronal cell types of all vertebrates tested. NeuN protein distributions are apparently restricted to neuronal nuclei, perikarya and some proximal neuronal processes in both fetal and adult brain although, some neurons fail to be recognized by NeuN at all ages: INL retinal cells, Cajal-Retzius cells, Purkinje cells, inferior olivary and dentate nucleus neurons, and sympathetic ganglion cells are examples (Mullen et al., 1992; Wolf et al., 1996). Immunohistochemically detectable NeuN protein first appears at developmental timepoints that correspond with the withdrawal of the neuron from the cell cycle and/or with the initiation of terminal differentiation of the neuron (Mullen et al., 1992). Immunoreactivity appears around E9.5 in the mouse neural tube and is extensive throughout the developing nervous system by E12.5. Strong nuclear staining suggests a nuclear regulatory protein function; however, no evidence currently exists as to whether the NeuN protein antigen has a function in the distal cytoplasm or whether it is merely synthesized there before being transported back into the nucleus. No difference between protein isolated from purified nuclei and whole brain extract on immunoblots has been found (Mullen et al., 1992). |
| Product Information | |
|---|---|
| Format | Purified |
| Control |
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| Presentation | Purified mouse immunoglobulin IgG1 liquid in buffer containing 0.02 M phosphate buffer, 0.25 M NaCl, pH 7.6 with 0.1% sodium azide. |
| Applications | |
|---|---|
| Application | Anti-NeuN Antibody, clone A60 detects level of NeuN and has been published and validated for use in FC, IC, IF, IH, IH(P), IP and WB. |
| Key Applications |
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| Application Notes | Western Blot Analysis: A previous lot of this antibody recognized 2-3 bands in the 46-48 kDa range and possibly another band at approximately 66 kDa. Immunocytochemistry: 1:10-1:100 dilution from a previous lot was used. Neurons in culture should be permeablized with 0.1% triton X-100. All primary antibody dilutions should be performed with simple solutions containing only buffer and primary antibody without excess protein blocks or detergents. Immunohistochemistry: 1:100-1:1,000. The antibody works best on polyester wax embedded tissue but also works on paraffin embedded tissue at a lower working dilution. The antibody works well with formaldehyde-based fixatives. Citric acid and microwave pretreatment has been used successfully (Sarnat, 1998). Immunohistochemistry(paraffin) Analysis: A previous lot was used for IH(P). Optimal working dilutions must be determined by end user. |
| Biological Information | |
|---|---|
| Immunogen | Purified cell nuclei from mouse brain |
| Clone | A60 |
| Concentration | Please refer to the Certificate of Analysis for the lot-specific concentration. |
| Host | Mouse |
| Specificity | MILLIPORE's exclusive monoclonal antibody to vertebrate neuron-specific nuclear protein called NeuN (or Neuronal Nuclei) reacts with most neuronal cell types throughout the nervous system of mice including cerebellum, cerebral cortex, hippocampus, thalamus, spinal cord and neurons in the peripheral nervous system including dorsal root ganglia, sympathetic chain ganglia and enteric ganglia. Developmentally, immunoreactivity is first observed shortly after neurons have become postmitotic, no staining has been observed in proliferative zones. The immunohistochemical staining is primarily localized in the nucleus of the neurons with lighter staining in the cytoplasm. The few cell types not reactive with MAB377 include Purkinje, mitral and photoreceptor cells. The antibody is an excellent marker for neurons in primary cultures and in retinoic acid-stimulated P19 cells. It is also useful for identifying neurons in transplants. |
| Isotype | IgG1 |
| Species Reactivity |
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| Antibody Type | Monoclonal Antibody |
| Gene Symbol |
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| Purification Method | Protein A Purfied |
| Molecular Weight | 46/48 kDa |
| Product Usage Statements | |
|---|---|
| Quality Assurance | Routinely evaluated by immunohistochemistry on brain tissue. Immunohistochemistry(paraffin) Analysis: NeuN (cat. # MAB377) staining pattern/morphology in rat cerebellum. Tissue pretreated with Citrate, pH 6.0. This lot of antibody was diluted to 1:100, using IHC-Select® Detection with HRP-DAB. Immunoreactivity is seen as nuclear staining in the neurons in the granular layer. Note that there is no signal detected in the nucleus of Purkinje cells. Optimal Staining With Citrate Buffer, pH 6.0, Epitope Retrieval: Rat Cerebellum |
| Usage Statement |
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| Storage and Shipping Information | |
|---|---|
| Storage Conditions | Stable for 6 months at 2-8ºC from date of receipt. |
| Packaging Information | |
|---|---|
| Material Size | 500 µg |
温馨提示：不可用于临床治疗。
