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Rabbit Anti-PHYHIP/AF594 Conjugated antibody
Rabbit Anti-PHYHIP/AF594 Conjugated antibody
LN1; PAHX; PhyH; PHYH; PHYH1; Phytanic acid oxidase; phytanoyl CoA 2 hydroxylase; Phytanoyl CoA 2 oxoglutarate dioxygenase; Phytanoyl CoA alpha hydroxylase; Phytanoyl CoA dioxygenase; RD antibody; PAHX_HUMAN; Phytanoyl-CoA dioxygenase, peroxisomal; Phytan
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Details

Product Name Anti-PHYHIP/AF594
Chinese Name AF594标记的植烷酸氧化酶抗体
Alias LN1; PAHX; PhyH; PHYH; PHYH1; Phytanic acid oxidase; phytanoyl CoA 2 hydroxylase; Phytanoyl CoA 2 oxoglutarate dioxygenase; Phytanoyl CoA alpha hydroxylase; Phytanoyl CoA dioxygenase; RD antibody; PAHX_HUMAN; Phytanoyl-CoA dioxygenase, peroxisomal; Phytanoyl-CoA alpha-hydroxylase.  
Research Area Tumour  Cell biology  immunology  Neurobiology  transcriptional regulatory factor  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Mouse, Rat, Dog, Cow, Rabbit, )
Applications IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Molecular weight 38kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human PHYH
Lsotype IgG
Purification affinity purified by Protein A
Storage Buffer 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
Product Detail 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.

Subunit:
Interacts specifically with the immunophilin FKBP52 and PHYHIP.

Subcellular Location:
Peroxisome.

Tissue Specificity:
Expressed in liver, kidney, and T-cells, but not in spleen, brain, heart, lung and skeletal muscle.

Similarity:
Belongs to the PhyH family.

Database links:

Entrez Gene: 5264 Human

Entrez Gene: 16922 Mouse

Entrez Gene: 114209 Rat

Omim: 602026 Human

SwissProt: O14832 Human

SwissProt: O35386 Mouse

SwissProt: P57093 Rat

Unigene: 498732 Human

Unigene: 391704 Mouse

Unigene: 7279 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

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