SPG7 Antikörper (AA 115-141)

Produktnummer ABIN656408

Der Kaninchen Polyklonal Anti-SPG7-Antikörper wurde für WB und IHC (p) validiert. Er ist geeignet, SPG7 in Proben von Human zu detektieren.

Kurzübersicht für SPG7 Antikörper (AA 115-141) (ABIN656408)

Target: SPG7 (Spastic Paraplegia 7 (SPG7))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SPG7 Antikörper ist unkonjugiert

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

Klon: RB23654

Produktdetails anti-SPG7 Antikörper

Bindungsspezifität: AA 115-141

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: WB: 1:1000. IHC-P: 1:10~50

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified polyclonal antibody 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: SPG7 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

Haltbarkeit: 6 months

Details zu SPG7

Target: SPG7 (Spastic Paraplegia 7 (SPG7))

Andere Bezeichnung: SPG7

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: 88235

Gen-ID: 6687

NCBI Accession: NP_003110, NP_955399

UniProt: Q9UQ90