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Congenital Stiff Person Syndrome: Disease Bioinformatics

Research of Congenital Stiff Person Syndrome has been linked to Hyperexplexia, Nervous System Disorder, Reflex, Abnormal, Muscle Rigidity, Muscle Hypertonia. The study of Congenital Stiff Person Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Congenital Stiff Person Syndrome include Startle Response, Localization. These pathways complement our catalog of research reagents for the study of Congenital Stiff Person Syndrome including antibodies and ELISA kits against INHIBITORY GLYCINE RECEPTOR, NEUROTRANSMITTER RECEPTOR, COLONY-STIMULATING FACTOR, CHRM1, CSF1R.

Top Research Reagents

We have 442 products for the study of Congenital Stiff Person Syndrome that can be applied to Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.

NB300-113
Western Blot: Glycine Receptor Alpha 1 Antibody [NB300-113] - Rat spinal cord lysate (SC) showing specific immunolabeling of the ~48 kDa alpha 1- and alpha 2-subunits of the glycine receptor. Immunolabeling was absent from a rat hippocampal lysate (H), as the glycine receptor is not expressed in the hippocampus.Western Blot: Glycine Receptor Alpha 1 Antibody [NB300-113] - Rat spinal cord showing specific immunolabeling of the ~48k a1- and a2-subunits of the glycine receptor. The labeling was absent from a Rat hippocampal (hipp) lysate as the glycine receptor is not expressed in the hippocampus.

Rabbit Polyclonal
Species Human, Mouse, Rat
Applications WB, IHC, IHC-Fr

4 Publications
NBP1-87466
Immunohistochemistry-Paraffin: Muscarinic Acetylcholine Receptor M1/CHRM1 Antibody [NBP1-87466] - Staining in human cerebral cortex and pancreas tissues using anti-CHRM1 antibody. Corresponding CHRM1 RNA-seq data are presented for the same tissues.Immunocytochemistry/Immunofluorescence: Muscarinic Acetylcholine Receptor M1/CHRM1 Antibody [NBP1-87466] - Staining of dissociated rat hippocampal culture. Image submitted by a verified customer review.

Rabbit Polyclonal
Species Human, Mouse, Rat
Applications WB, ICC/IF, IHC

     1 Review

5 Publications
NBP2-03449
Western Blot: Gephyrin/GPHN Antibody (3B6) [NBP2-03449] - Analysis of extracts (35ug) from 9 different cell lines by using anti-Gephyrin monoclonal antibody.Immunocytochemistry/Immunofluorescence: Gephyrin/GPHN Antibody (3B6) [NBP2-03449] -  Staining of COS7 cells transiently transfected by pCMV6-ENTRY Gephyrin.

Mouse Monoclonal
Species Human, Mouse, Rat
Applications WB, Flow, ICC/IF

     1 Review

NBP2-24716
Western Blot: MTSS1 Antibody [NBP2-24716] - Analysis of MTSS1 in human testis lysate in the 1) absence and 2) presence of immunizing peptide, 3) mouse and 4) rat testis lysate using NBP2-24716 at 2 ug/ml, 4 ug/ml and 2 ug/ml, respectively.Immunohistochemistry-Paraffin: MTSS1 Antibody [NBP2-24716] - Analysis of human colon using this antibody at 10 ug/ml.

Rabbit Polyclonal
Species Human, Mouse, Primate
Applications WB, ICC/IF, IHC

2 Publications
MAB3291
Western blot shows lysates of THP-1 human acute monocytic leukemia cell line. PVDF membrane was probed with 2 µg/mL of Mouse Anti-Human M-CSF R/CD115 Monoclonal Antibody (Catalog # MAB3291) followed by HRP-conjugated Anti-Mouse IgG Secondary Antibody (<a class=Recombinant Human M-CSF R/CD115 Fc Chimera (<a class=

Mouse Monoclonal
Species Human
Applications WB, IHC, Neut

11 Publications

Related Genes

Congenital Stiff Person Syndrome has been researched against:

Related Pathways

Congenital Stiff Person Syndrome has been linked to:

Alternate Names

Congenital Stiff Person Syndrome is also known as Familial Startle Disease, Stiff Baby Syndrome.