PHKG2 anticorps (N-Term)

N° du produit ABIN2777737

Cet anticorps anti-PHKG2 est un anticorps Lapin Polyclonal détectant PHKG2 dans WB et IHC. Adapté pour Humain, Souris, Rat, Chien, Boeuf (Vache), Chévre, Cobaye, Lapin, Mouton et Poisson zèbre (Danio rerio).

Aperçu rapide pour PHKG2 anticorps (N-Term) (ABIN2777737)

Antigène: PHKG2 (phosphorylase Kinase, gamma 2 (Testis) (PHKG2))

Reactivité: Humain, Souris, Rat, Chien, Boeuf (Vache), Chévre, Cobaye, Lapin, Mouton, Poisson zèbre (Danio rerio)

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PHKG2 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Détail du produit anti-PHKG2 anticorps

Épitope: N-Term

Séquence: EDELPDWAAA KEFYQKYDPK DVIGRGVSSV VRRCVHRATG HEFAVKIMEV

Homologie: Cow: 100%, Dog: 100%, Goat: 100%, Guinea Pig: 100%, Human: 100%, Mouse: 93%, Rabbit: 100%, Rat: 100%, Sheep: 100%, Zebrafish: 93%

Attributs du produit: This is a rabbit polyclonal antibody against PHKG2. It was validated on Western Blot and immunohistochemistry.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the N terminal region of human PHKG2

Information d'application

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

Commentaires:

Antigen size: 406 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 PHKG2

Antigène: PHKG2 (phosphorylase Kinase, gamma 2 (Testis) (PHKG2))

Autre désignation: PHKG2

Sujet: Mutations in PHKG2 along with PHKA2 and PHKB, all three different genes of phosphorylase kinase (Phk) subunits, can give rise to glycogen storage disease of the liver. The autosomal-recessive, liver-specific variant of Phk deficiency is caused by mutations in the gene encoding the testis/liver isoform of the catalytic gamma subunit, PHKG2.
Alias Symbols: GSD9C
Protein Interaction Partner: HAUS2, VCP, TP53, CDKN1A, UBC, PRKDC, PHKA2, PHKA1, ATAD3C, DRG1, NDUFA4, TNPO1, FASN, ACACA, GCN1L1, YME1L1, STUB1, SCO2, NPEPPS, VDAC2, ZC3H15, ATAD3A, BZW2, UBE3A, PHKG1,
Protein Size: 406

Poids moléculaire: 46 kDa

ID gène: 5261

NCBI Accession: NM_000294, NP_000285

UniProt: P15735

Pathways: Cellular Glucan Metabolic Process, Regulation of Carbohydrate Metabolic Process