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E-AB-15107

HSD17B4 Polyclonal Antibody

Size

£106.20

Was £118.00

SKU:
E-AB-15107
Additional Names:
12-alpha-trihydroxy-5-beta-cholest-24-enoyl-CoA hydratase,17 beta HSD 4,17 beta HSD IV,17 beta hydroxysteroid dehydrogenase 4,17-beta-HSD 4,17-beta-hydroxysteroid dehydrogenase 4,17beta estradiol dehydrogenase type IV,3 alpha 7 alpha12 alpha trihydroxy 5
Application:
IHC, WB
Concentration:
0.3 mg/ml
Purification:
Affinity Purified
Storage Conditions:
-20[o]C Avoid freeze/thaw cycles.
Supplier:
Elabscience
Host:
Rabbit
Reactivities:
Human, Mouse, Rat
Buffer:
Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
Immunogen:
Recombinant protein of human HSD17B4
Uniprot:
P51659
Synonyms:
17-beta-HSD 4;17-beta-HSD IV;17-beta-hydroxysteroid dehydrogenase 4;17beta-estradiol dehydrogenase type IV;3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholest-24-enoyl-CoA hydratase;beta-hydroxyacyl dehydrogenase;beta-keto-reductase;D-3-hydroxyacyl-CoA dehydratase;D-bifunctional protein;D-bifunctional protein, peroxisomal;DBP;epididymis secretory sperm binding protein;hydroxysteroid dehydrogenase 4;MFE-2;MFP-2;MPF-2;multifunctional protein 2;peroxisomal multifunctional enzyme type 2;peroxisomal multifunctional protein 2;PRLTS1;SDR8C1;short chain dehydrogenase/reductase family 8C member 1
Extra Details:
The protein encoded by this gene is a bifunctional enzyme that is involved in the peroxisomal beta-oxidation pathway for fatty acids.It also acts as a catalyst for the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids.Defects in this gene that affect the peroxisomal fatty acid beta-oxidation activity are a cause of D-bifunctional protein deficiency (DBPD).An apparent pseudogene of this gene is present on chromosome 8.
Shipping Conditions:
Blue Ice