catalog number :
MBS9216068
products full name :
SDHC Antibody (C-Term)
products short name :
[SDHC]
products name syn :
[Purified Rabbit Polyclonal Antibody (Pab); Succinate dehydrogenase cytochrome b560 subunit; mitochondrial; Integral membrane protein CII-3; QPs-1; QPs1; Succinate dehydrogenase complex subunit C; Succinate-ubiquinone oxidoreductase cytochrome B large subunit; CYBL; SDHC; CYB560; SDH3]
other names :
[succinate dehydrogenase cytochrome b560 subunit, mitochondrial isoform 2; Succinate dehydrogenase cytochrome b560 subunit, mitochondrial; succinate dehydrogenase cytochrome b560 subunit, mitochondrial; succinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa; Integral membrane protein CII-3; QPs-1; QPs1; Succinate dehydrogenase complex subunit C; Succinate-ubiquinone oxidoreductase cytochrome B large subunit; CYBL]
products gene name :
[SDHC]
other gene names :
[SDHC; SDHC; CYBL; PGL3; QPS1; SDH3; CYB560; CYB560; SDH3; QPs1; CYBL]
uniprot entry name :
C560_HUMAN
reactivity :
Human, Mouse
specificity :
This SDHC antibody is generated from a rabbit immunized with a KLH conjugated synthetic peptide between 113-144 amino acids from human SDHC.
form :
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
storage stability :
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
tested application :
Western Blot (WB), ELISA (EIA)
image1 heading :
Western Blot (WB)
other info1 :
Cellular location: Mitochondrion inner membrane; Multi-pass membrane protein. Calculated MW: 18610
products categories :
Cell Biology; Developmental Biology; Metabolism; Signal Transduction
products description :
Membrane-anchoring subunit of succinate dehydrogenase (SDH) that is involved in complex II of the mitochondrial electron transport chain and is responsible for transferring electrons from succinate to ubiquinone (coenzyme Q).
products references :
Au H.C.,et al.Submitted (MAY-1996) to the EMBL/GenBank/DDBJ databases. Hirawake H.,et al.Cytogenet. Cell Genet. 79:132-138(1997). Elbehti-Green A.,et al.Gene 213:133-140(1998). Wohllk N.,et al.Mol. Genet. Metab. 65:187-190(1998). Hiatomi H.,et al.Submitted (OCT-2005) to the EMBL/GenBank/DDBJ databases.
ncbi acc num :
NP_001030588.1
ncbi gb acc num :
NM_001035511.1
ncbi pathways :
Alzheimer's Disease Pathway (83097); Alzheimer's Disease Pathway (509); Biosynthesis Of Antibiotics Pathway (1144997); Carbon Metabolism Pathway (814926); Carbon Metabolism Pathway (817567); Citrate Cycle (TCA Cycle) Pathway (82927); Citrate Cycle (TCA Cycle) Pathway (288); Citric Acid Cycle (TCA Cycle) Pathway (1270125); Electron Transport Chain Pathway (198860); Huntington's Disease Pathway (83100)
ncbi summary :
This gene encodes one of four nuclear-encoded subunits that comprise succinate dehydrogenase, also known as mitochondrial complex II, a key enzyme complex of the tricarboxylic acid cycle and aerobic respiratory chains of mitochondria. The encoded protein is one of two integral membrane proteins that anchor other subunits of the complex, which form the catalytic core, to the inner mitochondrial membrane. There are several related pseudogenes for this gene on different chromosomes. Mutations in this gene have been associated with paragangliomas. Alternatively spliced transcript variants have been described. [provided by RefSeq, May 2013]
uniprot summary :
SDHC: Membrane-anchoring subunit of succinate dehydrogenase (SDH) that is involved in complex II of the mitochondrial electron transport chain and is responsible for transferring electrons from succinate to ubiquinone (coenzyme Q). Defects in SDHC are the cause of paragangliomas type 3 (PGL3). A neural crest tumor usually derived from the chromoreceptor tissue of a paraganglion. Paragangliomas are most commonly located in the head and neck region, specifically at the carotid bifurcation, the jugular foramen, the vagal nerve, and in the middle ear. Defects in SDHC are a cause of paraganglioma and gastric stromal sarcoma (PGGSS); also known as Carney- Stratakis syndrome. Gastrointestinal stromal tumors may be sporadic or inherited in an autosomal dominant manner, alone or as a component of a syndrome associated with other tumors, such as in the context of neurofibromatosis type 1 (NF1). Patients have both gastrointestinal stromal tumors and paragangliomas. Susceptibility to the tumors was inherited in an apparently autosomal dominant manner, with incomplete penetrance. Belongs to the cytochrome b560 family. 5 isoforms of the human protein are produced by alternative splicing. Protein type: Carbohydrate Metabolism - citrate (TCA) cycle; Energy Metabolism - oxidative phosphorylation; Membrane protein, integral; Membrane protein, multi-pass; Mitochondrial. Chromosomal Location of Human Ortholog: 1q23.3. Cellular Component: mitochondrial respiratory chain complex II; mitochondrion; mitochondrial inner membrane; integral to membrane. Molecular Function: succinate dehydrogenase (ubiquinone) activity; electron carrier activity; metal ion binding; heme binding. Biological Process: cellular metabolic process; mitochondrial electron transport, succinate to ubiquinone; tricarboxylic acid cycle; aerobic respiration. Disease: Gastrointestinal Stromal Tumor; Paraganglioma And Gastric Stromal Sarcoma; Paragangliomas 3