SPG7 Antikörper (AA 115-141)

Produktnummer ABIN5533448

Produktdetails anti-SPG7 Antikörper

Target: SPG7 (Spastic Paraplegia 7 (SPG7))

Bindungsspezifität: AA 115-141

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SPG7 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This SPG7 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 115-141 amino acids from the Central region of human SPG7.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: For WB starting dilution is: 1:1000

For IHC-P starting dilution is: 1:10~50

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: Store 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.

Details zu SPG7

Target: SPG7 (Spastic Paraplegia 7 (SPG7))

Andere Bezeichnung: SPG7 (SPG7 Produkte)

Synonyme: CAR antikoerper, CMAR antikoerper, PGN antikoerper, SPG5C antikoerper, AI452278 antikoerper, AU015315 antikoerper, Cmar antikoerper, SPG7, paraplegin matrix AAA peptidase subunit antikoerper, SPG7 antikoerper, Spg7 antikoerper

Hintergrund: This gene encodes a nuclear-encoded mitochondrial metalloprotease protein that is a member of the AAA (ATPases associated with a variety of cellular activities) protein family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. Two transcript variants encoding distinct isoforms have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 7. [provided by RefSeq].

Molekulargewicht: 88 kDa

Gen-ID: 6687

UniProt: Q9UQ90