GPD1 anticorps (Middle Region)

N° du produit ABIN2775306

Cet anticorps anti-GPD1 est un anticorps Lapin Polyclonal détectant GPD1 dans WB. Adapté pour Humain, Souris, Lapin, Rat, Chien, Cobaye, Cheval, Boeuf (Vache) et Saccharomyces cerevisiae.

Aperçu rapide pour GPD1 anticorps (Middle Region) (ABIN2775306)

Antigène: GPD1 (Glycerol-3-Phosphate Dehydrogenase 1 (Soluble) (GPD1))

Reactivité: Humain, Souris, Lapin, Rat, Chien, Cobaye, Cheval, Boeuf (Vache), Saccharomyces cerevisiae

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GPD1 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-GPD1 anticorps

Épitope: Middle Region

Séquence: TFLESCGVAD LITTCYGGRN RKVAEAFART GKSIEQLEKE LLNGQKLQGP

Homologie: Cow: 93%, Dog: 93%, Guinea Pig: 93%, Horse: 93%, Human: 100%, Mouse: 93%, Rabbit: 93%, Rat: 93%, Yeast: 93%

Attributs du produit: This is a rabbit polyclonal antibody against GPD1. It was validated on Western Blot using a cell lysate as a positive control.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the middle region of human GPD1

Information d'application

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

Commentaires:

Antigen size: 349 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 GPD1

Antigène: GPD1 (Glycerol-3-Phosphate Dehydrogenase 1 (Soluble) (GPD1))

Autre désignation: GPD1

Sujet: GPD1L belongs to the NAD-dependent glycerol-3-phosphate dehydrogenase family. Defects in GPD1L are the cause of Brugada syndrome type 2 (BRS2) and sudden infant death syndrome (SIDS).
Alias Symbols: FLJ26652, HTGTI
Protein Interaction Partner: GK, PTN, MDH1,
Protein Size: 349

Poids moléculaire: 37 kDa

ID gène: 2819

NCBI Accession: NM_005276, NP_005267

UniProt: P21695