543 Results for: "CLP"

Supplier: Bioss

A mutation of the DYT1 gene, which codes for TorsinA, has been identified as the cause of one form of autosomal dominantly inherited dystonia. Early-onset torsion dystonia is a movement disorder, characterized by twisting muscle contractures, that begins in childhood. Symptoms are believed to result from altered neuronal communication in the basal ganglia. TorsinA comprises 332 amino acids. TorsinA is widely expressed throughout the mouse central nervous system and is detected in the majority of neurons in nearly all regions. The proteins display cytoplasmic distribution, although in some types of neurons localization is perinuclear. TorsinA often performs chaperone-like functions that assist in the assembly, operation, or dis-assembly of protein complexes. The gene which encodes TorsinA has high homology to three additional mammalian genes and a nematode gene and distal similarity to the family of heat-shock proteins and the Clp protease family. The gene which encodes TorsinA maps to human chromosome 9q34.

Supplier: Molekula

Chlorodiphenylphosphine

Supplier: Merck

Tetraphenylphosphonium chloride, Sigma-Aldrich®

Supplier: Thermo Scientific

Allyltriphenylphosphonium chloride

Supplier: Merck

Dicyclopentylchlorophosphine, Sigma-Aldrich®

Supplier: Molekula

Allyltriphenylphosphonium chloride

Supplier: Bioss

A mutation of the DYT1 gene, which codes for TorsinA, has been identified as the cause of one form of autosomal dominantly inherited dystonia. Early-onset torsion dystonia is a movement disorder, characterized by twisting muscle contractures, that begins in childhood. Symptoms are believed to result from altered neuronal communication in the basal ganglia. TorsinA comprises 332 amino acids. TorsinA is widely expressed throughout the mouse central nervous system and is detected in the majority of neurons in nearly all regions. The proteins display cytoplasmic distribution, although in some types of neurons localization is perinuclear. TorsinA often performs chaperone-like functions that assist in the assembly, operation, or dis-assembly of protein complexes. The gene which encodes TorsinA has high homology to three additional mammalian genes and a nematode gene and distal similarity to the family of heat-shock proteins and the Clp protease family. The gene which encodes TorsinA maps to human chromosome 9q34.

Supplier: Bioss

A mutation of the DYT1 gene, which codes for TorsinA, has been identified as the cause of one form of autosomal dominantly inherited dystonia. Early-onset torsion dystonia is a movement disorder, characterised by twisting muscle contractures, that begins in childhood. Symptoms are believed to result from altered neuronal communication in the basal ganglia. TorsinA comprises 332 amino acids. TorsinA is widely expressed throughout the mouse central nervous system and is detected in the majority of neurons in nearly all regions. The proteins display cytoplasmic distribution, although in some types of neurons localisation is perinuclear. TorsinA often performs chaperone-like functions that assist in the assembly, operation, or dis-assembly of protein complexes. The gene which encodes TorsinA has high homology to three additional mammalian genes and a nematode gene and distal similarity to the family of heat-shock proteins and the Clp protease family. The gene which encodes TorsinA maps to human chromosome 9q34.

Supplier: Merck

Chloro(diisopropyl)phosphine, Sigma-Aldrich®

Supplier: Thermo Scientific

Benzyl(tributyl)phosphonium chloride

Supplier: Bioss

A mutation of the DYT1 gene, which codes for TorsinA, has been identified as the cause of one form of autosomal dominantly inherited dystonia. Early-onset torsion dystonia is a movement disorder, characterized by twisting muscle contractures, that begins in childhood. Symptoms are believed to result from altered neuronal communication in the basal ganglia. TorsinA comprises 332 amino acids. TorsinA is widely expressed throughout the mouse central nervous system and is detected in the majority of neurons in nearly all regions. The proteins display cytoplasmic distribution, although in some types of neurons localization is perinuclear. TorsinA often performs chaperone-like functions that assist in the assembly, operation, or dis-assembly of protein complexes. The gene which encodes TorsinA has high homology to three additional mammalian genes and a nematode gene and distal similarity to the family of heat-shock proteins and the Clp protease family. The gene which encodes TorsinA maps to human chromosome 9q34.

Supplier: Bioss

A mutation of the DYT1 gene, which codes for TorsinA, has been identified as the cause of one form of autosomal dominantly inherited dystonia. Early-onset torsion dystonia is a movement disorder, characterised by twisting muscle contractures, that begins in childhood. Symptoms are believed to result from altered neuronal communication in the basal ganglia. TorsinA comprises 332 amino acids. TorsinA is widely expressed throughout the mouse central nervous system and is detected in the majority of neurons in nearly all regions. The proteins display cytoplasmic distribution, although in some types of neurons localisation is perinuclear. TorsinA often performs chaperone-like functions that assist in the assembly, operation, or dis-assembly of protein complexes. The gene which encodes TorsinA has high homology to three additional mammalian genes and a nematode gene and distal similarity to the family of heat-shock proteins and the Clp protease family. The gene which encodes TorsinA maps to human chromosome 9q34.

Supplier: ANTIBODIES.COM

Mouse Clps ELISA kit is a 90 minutes sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse Clps in serum, plasma, and other biological fluids.

Supplier: Thermo Scientific

(2,3,4,5,6-Pentamethylbenzyl)tripropylphosphonium chloride

Supplier: Thermo Scientific

(2,3,4,5,6-Pentamethylbenzyl)triphenylphosphonium chloride

Supplier: Merck

Chloro(diethyl)phosphine, Sigma-Aldrich®

Supplier: Merck

Dicyclohexylchlorophosphine, Sigma-Aldrich®

Supplier: Restek

Organic Standard, CLP VOA CAL2000 MegaMix standard, 1 ml/ampoule

Supplier: Merck

Trihexyl(tetradecyl)phosphonium chloride, Sigma-Aldrich®

Supplier: Merck

Chlorodiphenylphosphine, Sigma-Aldrich®

Supplier: Merck

Chlorobis(2-methylphenyl)phosphine, Sigma-Aldrich®

Supplier: Abnova

Anti-CLPS Mouse Polyclonal Antibody

Supplier: Abnova

Anti-CLPS Rabbit Polyclonal Antibody

Supplier: ANTIBODIES.COM

Human Cathelicidin/CLP ELISA kit is a 90 minute sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human Cathelicidin/CLP in serum, plasma, and other biological fluids.

Supplier: ANTIBODIES.COM

Mouse Cathelicidin/CLP ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse Cathelicidin/CLP in serum, plasma, tissue homogenates, and other biological fluids.

Supplier: ANTIBODIES.COM

Human Cathelicidin/CLP ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human Cathelicidin/CLP in serum, plasma, tissue homogenates, and other biological fluids.

Supplier: ANTIBODIES.COM

Rabbit polyclonal antibody to Cathelicidin / CLP for WB and IHC with samples derived from human and mouse.

Supplier: ANTIBODIES.COM

Rabbit polyclonal antibody to Cathelicidin/CLP for WB, IHC and ICC/IF with samples derived from Human and Rat.

Supplier: Restek

This contains atrazine, benzaldehyde and ε-caprolactam.

Supplier: ANTIBODIES.COM

Rabbit polyclonal antibody to CLPS for WB with samples derived from human and mouse.