PMP22 Antikörper (N-Term)

Produktnummer ABIN2789416

Dieser Anti-PMP22 Antikörper ist ein Kaninchen Polyklonal Antikörper zur Detektion von PMP22 in WB. Geeignet für Human, Ratte, Rind (Kuh), Meerschweinchen, Kaninchen, Hund, Pferd und Schaf.

Kurzübersicht für PMP22 Antikörper (N-Term) (ABIN2789416)

Target: PMP22 (Peripheral Myelin Protein 22 (PMP22))

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

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PMP22 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-PMP22 Antikörper

Bindungsspezifität: N-Term

Sequenz: QWIVGNGHAT DLWQNCSTSS SGNVHHCFSS SPNEWLQSVQ ATMILSIIFS

Homologie: Cow: 100%, Dog: 93%, Guinea Pig: 100%, Horse: 86%, Human: 100%, Rabbit: 100%, Rat: 93%, Sheep: 86%

Produktmerkmale: This is a rabbit polyclonal antibody against PMP22. It was validated on Western Blot.

Aufreinigung: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the N-terminal region of PMP22

Anwendungsinformationen

Applikationshinweise: Optimal working dilutions should be determined experimentally by the investigator.

Kommentare:

Antigen size: 160 AA

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: Lot specific

Buffer: Liquid. 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: Avoid repeated freeze-thaw cycles.

Lagerung: -20 °C

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

Details zu PMP22

Target: PMP22 (Peripheral Myelin Protein 22 (PMP22))

Andere Bezeichnung: PMP22

Hintergrund: This gene encodes an integral membrane protein that is a major component of myelin in the peripheral nervous system. Various mutations of this gene are causes of Charcot-Marie-Tooth disease Type IA, Dejerine-Sottas syndrome, and hereditary neuropathy with liability to pressure palsies. Alternative splicing of this gene results in three transcript variants that encode the same protein.
Alias Symbols: CMT1A, CMT1E, DSS, GAS-3, HMSNIA, HNPP, MGC20769, Sp110
Protein Interaction Partner: SMIM3, KLRC1, PEX19, DDX52, ELAVL1, MPZ, CANX,
Protein Size: 160

Molekulargewicht: 18 kDa

Gen-ID: 5376

NCBI Accession: NM_153321, NP_696996

UniProt: Q01453