Product Name
phytanoyl-CoA 2-hydroxylase (PHYH), ELISA Kit
Full Product Name
Rat Phytanoyl-CoA dioxygenase, peroxisomal, PHYH ELISA Kit
Product Synonym Names
Rat Phytanoyl-CoA dioxygenase; peroxisomal (PHYH) ELISA kit; RP11-24J20.1; LN1; LNAP1; PAHX; PHYH1; RD; phytanic acid oxidase; phytanoil-CoA alpha hydroxylase; phytanoyl-CoA 2 oxoglutarate dioxygenase; phytanoyl-CoA alpha-hydroxylase; phytanoyl-CoA dioxygenase; p; phytanoyl-CoA 2-hydroxylase
Product Gene Name
PHYH elisa kit
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Request for Current Manual Insert
Request Current Manual
3D Structure
ModBase 3D Structure for P57093
Preparation and Storage
Store all reagents at 2-8 degree C
Product Note
Select online data sheet information is drawn from bioinformatics databases, occasionally resulting in ambiguous or non-relevant product information. It is the responsibility of the customer to review, verify, and evaluate the information to make sure it matches their requirements before purchasing the kit. Our ELISA Kit assays are dynamic research tools and sometimes they may be updated and improved. If the format of this assay is important to you then please request the current manual or contact our technical support team with a presales inquiry before placing an order. We will confirm the current details of the assay. We cannot guarantee the sample manual posted online is the most current manual.
Other Notes
Small volumes of PHYH elisa kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Searchable Terms for PHYH purchase
MBS9333846 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the phytanoyl-CoA 2-hydroxylase (PHYH) ELISA Kit target analytes in
biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing PHYH. The ELISA analytical biochemical technique of the MBS9333846 kit is based on PHYH antibody-PHYH antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect PHYH antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, PHYH. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).
NCBI/Uniprot data below describe general gene information for PHYH. It may not necessarily be applicable to this product.
NCBI Accession #
NP_446126.1
[Other Products]
NCBI GenBank Nucleotide #
NM_053674.1
[Other Products]
UniProt Primary Accession #
P57093
[Other Products]
UniProt Secondary Accession #
Q9QY64[Other Products]
UniProt Related Accession #
P57093[Other Products]
Molecular Weight
38,588 Da
NCBI Official Full Name
phytanoyl-CoA dioxygenase, peroxisomal
NCBI Official Synonym Full Names
phytanoyl-CoA 2-hydroxylase
NCBI Official Symbol
Phyh [Similar Products]
NCBI Protein Information
phytanoyl-CoA dioxygenase, peroxisomal; phytanic acid oxidase; phytanoyl-CoA alpha-hydroxylase; phytanoyl-CoA hydroxylase (Refsum disease)
UniProt Protein Name
Phytanoyl-CoA dioxygenase, peroxisomal
UniProt Synonym Protein Names
Phytanic acid oxidase; Phytanoyl-CoA alpha-hydroxylase; PhyH
Protein Family
Phytanoyl-CoA dioxygenase
UniProt Gene Name
Phyh [Similar Products]
UniProt Synonym Gene Names
PhyH [Similar Products]
UniProt Entry Name
PAHX_RAT
NCBI Summary for PHYH
catalyzes the conversion of phytanoyl-CoA to 2-hydroxyphytanoyl-CoA; plays a role in phytanic acid alpha-oxidation [RGD, Feb 2006]
UniProt Comments for PHYH
PHYH: Converts phytanoyl-CoA to 2-hydroxyphytanoyl-CoA. Defects in PHYH are a cause of Refsum disease (RD). RD is an autosomal recessive disorder characterized clinically by a tetrad of abnormalities: retinitis pigmentosa, peripheral neuropathy, cerebellar ataxia, and elevated protein levels in the cerebrospinal fluid (CSF). Patients exhibit accumulation of the branched-chain fatty acid, phytanic acid, in blood and tissues. Less constant features are nerve deafness, anosmia, skeletal abnormalities, ichthyosis, cataracts and cardiac impairment. Manifestations of the disease appear in the second or third decade of life. Belongs to the PhyH family.
Protein type: Oxidoreductase; EC 1.14.11.18
Cellular Component: mitochondrion; peroxisome
Molecular Function: L-ascorbic acid binding; metal ion binding; cofactor binding; catalytic activity; phytanoyl-CoA dioxygenase activity
Biological Process: isoprenoid metabolic process; fatty acid alpha-oxidation
Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.
It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.