PHYH antibody (AA 1-338)

Catalog No. ABIN6145582

Product Details anti-PHYH Antibody

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

Binding Specificity: AA 1-338

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PHYH antibody is un-conjugated

Application: Western Blotting (WB)

Sequence: 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

Cross-Reactivity: Human, Mouse

Characteristics: Polyclonal Antibodies

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

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000

Restrictions: For Research Use only

Handling

Format: Liquid

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

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for PHYH

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

Alternative Name: PHYH (PHYH Products)

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

Background: 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

Molecular Weight: 27 kDa/38 kDa

Gene ID: 5264

UniProt: O14832

Pathways: Monocarboxylic Acid Catabolic Process