PHYH anticorps (AA 1-338)

N° du produit ABIN6145582

Détail du produit anti-PHYH anticorps

Antigène: PHYH (Phytanoyl-CoA 2-Hydroxylase (PHYH))

Épitope: AA 1-338

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PHYH est non-conjugé

Application: Western Blotting (WB)

Séquence: MEQLRAAARL QIVLGHLGRP SAGAVVAHPT SGTISSASFH PQQFQYTLDN NVLTLEQRKF YEENGFLVIK NLVPDADIQR FRNEFEKICR KEVKPLGLTV MRDVTISKSE YAPSEKMITK VQDFQEDKEL FRYCTLPEIL KYVECFTGPN IMAMHTMLIN KPPDSGKKTS RHPLHQDLHY FPFRPSDLIV CAWTAMEHIS RNNGCLVVLP GTHKGSLKPH DYPKWEGGVN KMFHGIQDYE ENKARVHLVM EKGDTVFFHP LLIHGSGQNK TQGFRKAISC HFASADCHYI DVKGTSQENI EKEVVGIAHK FFGAENSVNL KDIWMFRARL VKGERTNL

Réactivité croisée: Humain, Souris

Attributs du produit: Polyclonal Antibodies

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 1-338 of human PHYH (NP_006205.1).

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 PHYH

Antigène: PHYH (Phytanoyl-CoA 2-Hydroxylase (PHYH))

Autre désignation: PHYH (PHYH Produits)

Synonymes: anticorps zgc:110203, anticorps LN1, anticorps LNAP1, anticorps PAHX, anticorps PHYH1, anticorps RD, anticorps AI256161, anticorps AI265699, anticorps Lnap1, anticorps phytanoyl-CoA 2-hydroxylase, anticorps phytanoyl-CoA hydroxylase-like, anticorps phytanoyl-CoA hydroxylase, anticorps PHYH, anticorps LOC478001, anticorps phyh, anticorps Phyh

Sujet: This gene is a member of the PhyH family and encodes a peroxisomal protein that is involved in the alpha-oxidation of 3-methyl branched fatty acids. Specifically, this protein converts phytanoyl-CoA to 2-hydroxyphytanoyl-CoA. Mutations in this gene have been associated with Refsum disease (RD) and deficient protein activity has been associated with Zellweger syndrome and rhizomelic chondrodysplasia punctata. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.,PHYH,LN1,LNAP1,PAHX,PHYH1,RD,Epigenetics & Nuclear Signaling,Cancer,Signal Transduction,Endocrine & Metabolism,Lipid Metabolism,Neuroscience,PHYH

Poids moléculaire: 27 kDa/38 kDa

ID gène: 5264

UniProt: O14832

Pathways: Monocarboxylic Acid Catabolic Process