SLC6A8 anticorps (AA 539-635)

N° du produit ABIN7270473

Détail du produit anti-SLC6A8 anticorps

Antigène: SLC6A8 (Solute Carrier Family 6 (Neurotransmitter Transporter, Creatine), Member 8 (SLC6A8))

Épitope: AA 539-635

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SLC6A8 est non-conjugé

Application: Western Blotting (WB)

Fonction: SLC6A8 Rabbit pAb

Séquence: VVYYEPLVYN NTYVYPWWGE AMGWAFALSS MLCVPLHLLG CLLRAKGTMA ERWQHLTQPI WGLHHLEYRA QDADVRGLTT LTPVSESSKV VVVESVM

Réactivité croisée: Humain, Souris

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 539-635 of human SLC6A8 (NP_005620.1).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

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.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur SLC6A8

Antigène: SLC6A8 (Solute Carrier Family 6 (Neurotransmitter Transporter, Creatine), Member 8 (SLC6A8))

Autre désignation: SLC6A8 (SLC6A8 Produits)

Synonymes: anticorps SLC6A8, anticorps chot1, anticorps crtr, anticorps creaT, anticorps CHOT1, anticorps CHT1, anticorps CRT, anticorps CT1, anticorps AA589632, anticorps CRTR, anticorps Creat, anticorps CCDS1, anticorps solute carrier family 6 member 8, anticorps sodium- and chloride-dependent creatine transporter 1, anticorps solute carrier family 6 (neurotransmitter transporter), member 8, anticorps solute carrier family 6 (neurotransmitter transporter, creatine), member 8, anticorps SLC6A8, anticorps LOC473853, anticorps slc6a8, anticorps LOC100440816, anticorps Slc6a8

Sujet: The protein encoded by this gene is a plasma membrane protein whose function is to transport creatine into and out of cells. Defects in this gene can result in X-linked creatine deficiency syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008],CCDS1,CRT,CRTR,CT1,CTR5,SLC6A8,Cancer,Signal Transduction,Endocrine & Metabolism,SLC6A8

Poids moléculaire: 30kDa/58kDa/70kDa/80kDa

ID gène: 6535

UniProt: P48029

Pathways: Retinoic Acid Receptor Signaling Pathway, Intracellular Steroid Hormone Receptor Signaling Pathway, Regulation of Intracellular Steroid Hormone Receptor Signaling, Nuclear Hormone Receptor Binding, ER-Nucleus Signaling, Unfolded Protein Response