CLN5 Antikörper (C-Term)

Produktnummer ABIN5517800

Der Kaninchen Polyklonal anti-CLN5 Antikörper (ABIN5517800) detektiert spezifisch CLN5. Dieser Antikörper reagiert spezifisch mit Proben aus Human, Ratte, Rind (Kuh), Hund, Meerschweinchen, Pferd, Schwein und Kaninchen.

Kurzübersicht für CLN5 Antikörper (C-Term) (ABIN5517800)

Target: CLN5 (Ceroid-Lipofuscinosis, Neuronal 5 (CLN5))

Reaktivität: Human, Ratte, Rind (Kuh), Hund, Meerschweinchen, Pferd, Schwein, Kaninchen

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CLN5 Antikörper ist unkonjugiert

Applikation: Bitte anfragen

Produktdetails anti-CLN5 Antikörper

Bindungsspezifität: C-Term

Verwendungszweck: CLN5 Antibody - C-terminal region

Sequenz: DNETGIYYET WNVKASPEKG AETWFDSYDC SKFVLRTFNK LAEFGAEFKN

Homologie: Cow: 77%, Dog: 79%, Guinea Pig: 79%, Horse: 86%, Human: 100%, Pig: 86%, Rabbit: 86%, Rat: 79%

Aufreinigung: Affinity purified

Immunogen: The immunogen is a synthetic peptide directed towards the C terminal region of human CLN5

Anwendungsinformationen

Kommentare:

We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP59986-100UG

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.5 mg/mL

Buffer: Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Konservierungsmittel: Sodium azide

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

Handhabung: prevent freeze-thaw cycles

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Details zu CLN5

Target: CLN5 (Ceroid-Lipofuscinosis, Neuronal 5 (CLN5))

Andere Bezeichnung: CLN5

Hintergrund:

Background Information: This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function.

Gene Name: ceroid-lipofuscinosis, neuronal 5

Alternative Symbols: NCL

Protein Name: ceroid-lipofuscinosis neuronal protein 5

Molekulargewicht: 39 kDa

Gen-ID: 1203

NCBI Accession: NP_006484

UniProt: O75503