PMP22 anticorps (N-Term)

N° du produit ABIN2789416

Cet anticorps anti-PMP22 est un anticorps Lapin Polyclonal détectant PMP22 dans WB. Adapté pour Humain, Rat, Boeuf (Vache), Cobaye, Lapin, Chien, Cheval et Mouton.

Aperçu rapide pour PMP22 anticorps (N-Term) (ABIN2789416)

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

Reactivité: Humain, Rat, Boeuf (Vache), Cobaye, Lapin, Chien, Cheval, Mouton

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PMP22 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-PMP22 anticorps

Épitope: N-Term

Séquence: QWIVGNGHAT DLWQNCSTSS SGNVHHCFSS SPNEWLQSVQ ATMILSIIFS

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

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

Purification: Affinity Purified

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

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator.

Commentaires:

Antigen size: 160 AA

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: Lot specific

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

Agent conservateur: Sodium azide

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

Conseil sur la manipulation: Avoid repeated freeze-thaw cycles.

Stock: -20 °C

Stockage commentaire: 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.

Détails sur PMP22

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

Autre désignation: PMP22

Sujet: 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

Poids moléculaire: 18 kDa

ID gène: 5376

NCBI Accession: NM_153321, NP_696996

UniProt: Q01453