
SDHD Antilichaam
Kwaliteit
ISO Gecertificeerd
Levering
24-48 uur
Technische Specificaties
SDHD Antibody: The mitochondrial succinate dehydrogenase complex subunit D (SDHD) is one of four proteins that make up the tricarboxylic cycle enzyme succinate dehydrogenase (SCH) . Studies have shown that mutations in SDHD often leads to hereditary paragangliomas, usually benign tumors of the autonomic nervous system, suggesting that SDHD also plays a role as a tumor-suppressor gene. In one family with a nonsense mutation (R22X) in the SDHD gene, a loss of heterozygosity was found in the paragangliomas, and within these tumors the enzymatic activity of Complex II in the mitochondrial respiratory chain was completely abolished. Furthermore, high levels of angiogenic factors EPAS1 and VEGF was observed, which may stimulate tumor growth.
9392
O14521
NP_002993
• Rabbit
Human, Mouse, Rat
• Polyclonal
Unconjugated
Primary Antibodies
Cancer, Cell Cycle
SDHD Antibody is affinity chromatography purified via peptide column.
Cat. No. 1287 - EL4 Cell Lysate
1 mg/mL
Predicted species reactivity based on immunogen sequence: Bovine: (100%), Sheep: (100%), Pig: (80%)
SDHD Antibody is supplied in PBS containing 0.02% sodium azide.
None
Blue Ice
SDHD antibody can be stored at 4˚ C for three months and -20˚ C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
IgG
At least four isoforms of SDHD are known to exist; this antibody will detect the two longest isoforms.
SDHD
Cat. No. 17-207 - EL4 Cell Slide
Succinate dehydrogenase complex, subunit D, integral membrane protein
Homo sapiens
Baysal BE, Ferrell RE, Willett-Brozick JE, et al. Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. Science 2000; 287:848-51.
Saraste M. Oxidative phosphorylation at the fin de siecle. Science 1999; 283:1488-93.
Knudson AG. Genetics of human cancer. Annu. Rev. Genet. 1986; 20:231-51.
Gimenez-Roqueplo AP, Favier J, Rustin P, et al. The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of Complex II in the mitochondrial respiratory chain and activates the hypoxia pathway. Am. J. Hum. Genet. 2001; 69:1186-97.
SDHD Antibody: TRAP1, TRAP-1, SDH4, CII-4, CybS
ELISA, WB, ICC, IF
4506865
Liquid
Beschrijving
SDHD Antilichaam Beschikbaar in 0.02 mg. Bestel eenvoudig online met snelle levering.
Specificaties
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