Thermo Fisher Scientific AGPS Polyclonal Antibody

Applications

Tested Dilution

Publications

Western Blot (WB)

1:1,000-1:2,000

-

Immunocytochemistry (ICC/IF)

1:50-1:200

-

ELISA (ELISA)

1 µg/mL

-

Product Specifications

Species Reactivity

Human, Mouse

Host/Isotype

Rabbit / IgG

Class

Polyclonal

Type

Antibody

Immunogen

Recombinant fusion protein containing a sequence corresponding to amino acids 379-658 of human AGPS (NP_0036501) if (typeof window.$mangular === undefined || !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{targetFamily:AGPS,uniProtId:O00116-1,ncbiNodeId:9606,antigenRange:379-658,antigenLength:658,antigenImageFileName:PA5-87935_AGPS_O00116-1_Rabbit.svg,antigenImageFileNamePDP:PA5-87935_AGPS_O00116-1_Rabbit_PDP.jpeg,sortOrder:1}\]; $mangular.isB2BCMGT = false; $mangular.isEpitopesModalImageMultiSizeEnabled = true;

View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

3.66 mg/mL

Purification

Affinity Chromatography

Storage buffer

PBS, pH 7.3, with 50% glycerol

Contains

0.02% sodium azide

Storage conditions

-20° C, Avoid Freeze/Thaw Cycles

Shipping conditions

Wet ice

RRID

AB_2804518

Product Specific Information

Immunogen sequence: IKIRPVPEYQ KYGSVAFPNF EQGVACLREI AKQRCAPASI RLMDNKQFQF GHALKPQVSS IFTSFLDGLK KFYITKFKGF DPNQLSVATL LFEGDREKVL QHEKQVYDIA AKFGGLAAGE DNGQRGYLLT YVIAYIRDLA LEYYVLGESF ETSAPWDRVV DLCRNVKERI TRECKEKGVQ FAPFSTCRVT QTYDAGACIY FYFAFNYRGI SDPLTVFEQT EAAAREEILA NGGSLSHHHG VGKLRKQWLK ESISDVGFGM LKSVKEYVDP NNIFGNRNLL; Positive Samples: HL-60, HeLa, HepG2, K-562, Mouse kidney, Mouse lung; Cellular Location: Peroxisome membrane

Target Information

This gene is a member of the FAD-binding oxidoreductase/transferase type 4 family. It encodes a protein that catalyzes the second step of ether lipid biosynthesis in which acyl-dihydroxyacetonephosphate (DHAP) is converted to alkyl-DHAP by the addition of a long chain alcohol and the removal of a long-chain acid anion. The protein is localized to the inner aspect of the peroxisomal membrane and requires FAD as a cofactor. Mutations in this gene have been associated with rhizomelic chondrodysplasia punctata, type 3 and Zellweger syndrome.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.