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C9orf72 Antibody

Catalogue number:
200-901-MH2S
Size:
25 µl
Product is available in:
  • UK
  • Ireland
  • Europe
  • USA
  • Rest of World
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Applications:

ELISA, Flow Cytometry, Immunohistochemistry, IF Microscopy

Antibody Host:

Chicken

Species Reactivity:

H. sapiens (Human)

Antibody Isotype:

IgY

Antibody Type:

Polyclonal

Immunogen:

Anti-C9orf72 antibody was prepared from eggs of chickens laid after repeated immunizations with a synthetic peptide corresponding to a C-terminal port

Alternative Names:

Chicken Anti-Chromosome 9 Open Reading Frame 72 Antibody, Chicken Anti-C9orf72 Antibody, Guanine Nucleotide Exchange, Protein C9orf72, DENNL72, FTDALS1, ALSFTD, FTDALS

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Product Description:

C9orf72 (Chromosome 9 Open Reading Frame 72) plays an important role in the regulation of endosomal trafficking and has been shown to interact with Rab proteins that are involved in autophagy and endocytic transport. It is a component of the C9orf72-SMCR8 complex, a complex that has guanine nucleotide exchange factor (GEF) activity and regulates autophagy. In the complex, C9orf72 and SMCR8 probably constitute the catalytic subunits that promote the exchange of GDP to GTP, converting inactive GDP-bound RAB8A and RAB39B into their active GTP-bound form, thereby promoting autophagosome maturation. The C9orf72-SMCR8 complex also acts as a regulator of autophagy initiation by interacting with the ATG1/ULK1 kinase complex and modulating its protein kinase activity. It positively regulates initiation of autophagy by regulating the RAB1A-dependent trafficking of the ATG1/ULK1 kinase complex to the phagophore which leads to autophagosome formation. And acts as a regulator of mTORC1 signaling by promoting phosphorylation of mTORC1 substrates. C9orf72 may be involved in regulating the maturation of phagosomes to lysosomes. It regulates actin dynamics in motor neurons by inhibiting the GTP-binding activity of ARF6, leading to ARF6 inactivation. This reduces the activity of the LIMK1 and LIMK2 kinases which are responsible for phosphorylation and inactivation of cofilin, leading to cofilin activation. It positively regulates axon extension and axon growth cone size in spinal motor neurons. C9orf72 plays a role within the hematopoietic system in restricting inflammation and the development of autoimmunity. Studies suggest that hexanucleotide expansions could result in the selective stabilization of repeat-containing pre-mRNA, and the accumulation of insoluble dipeptide repeat protein aggregates that could be pathogenic in FTD-ALS patients. Diseases associated with C9orf72 include Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1 and Huntington Disease-Like Syndrome Due To C9orf72 Expansions. Anti-C9orf72 Antibody is useful for researchers interested in Neuroscience Research. Anti-C9orf72 Antibody has been tested in Immunohistochemistry, Immunofluorescence, and Flow Cytometry. Western blot not recommended. Positive control used: Human cerebellum in IHC, U2-OS in IF, MCF7 in FLOW.

Immunofluorescence of Chicken Anti-C9orf
Immunofluorescence of Chicken Anti-C9orf72 Antibody. Cells: U2-OS Cells. Fixative: 4% PFA. Permeabilization: 0.3% Triton X-100. Primary Antibody: Anti-C9orf72 at 5µg/mL overnight at 2-8°C. Secondary Antibody: Goat Anti-Chicken IgG DyLight™488 (p/n 603-141-126) at 15µg/mL for 1hr at RT. Nuclear Counterstain: DAPI. Staining: (A) DAPI. (B) C9orf72 and secondary DyLight™488. (C) Merge A+B. (D) secondary only. Predicted localization: Nucleous, Endosome, Lysosome, Extracellular region or secreted. Image has been deconvoluted. Punctate staining may be indicative of endosomes in the cytoplasmic cell compartment.
Immunohistochemistry of Chicken Anti-C9o
Immunohistochemistry of Chicken Anti-C9orf72 Antibody. Tissue: Human Cerebellum. Fixative: None. Antigen Retrieval: HIER using citrate buffer for 20 min. Primary Antibody: Anti-C9orf72 at 1:200 for 30 min at RT. Secondary Antibody: Alpha Anti Chicken HRP at 1:500 for 20 min at RT. Counterstain: Hematoxylin. Substrate: DAB. Analysis Results: C9ORF72 shows intense staining at a dilution of 1:100 and 1:200 of vascular endothelial cells, low intensity staining of neurophil and occasional more intense staining of glial cells. The specificity of this pattern of staining is consistent with C9ORF72 staining in the databases for cerebellum.