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HPGD antibody
HPGD
Reactivity: Mouse
IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-HPGD Antibody
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Target
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HPGD
(Hydroxyprostaglandin Dehydrogenase 15-(NAD) (HPGD))
Reactivity
All reactivities for HPGD antibodies
Mouse
Host
All hosts for HPGD antibodies
Rabbit
Clonality
All clonalities for HPGD antibodies
Polyclonal
Conjugate
All conjugates for HPGD antibodies
This HPGD antibody is un-conjugated
Application
All applications for HPGD antibodies
Immunohistochemistry (IHC)
Characteristics
Polyclonal Antibody
Purification
Antigen Affinity Purification
Immunogen
Recombinant Mouse 15-hydroxyprostaglandin dehydrogenase [NAD(+)] protein
Isotype
IgG
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Discover our top product HPGD Primary Antibody
Alternatives
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Application Details
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Application Notes
IHC 1:100-1:200
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
0.69 mg/mL
Buffer
PBS with 0.05 % Proclin300 and 50 % glycerol, pH 7.4.
Preservative
ProClin
Precaution of Use
This product contains ProClin: 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 HPGD
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Target
HPGD
(Hydroxyprostaglandin Dehydrogenase 15-(NAD) (HPGD))
Alternative Name
HPGD (HPGD Products )
Synonyms
CBR antibody, SDR21C1 antibody, hCBR1 antibody, 15-PGDH antibody, PGDH antibody, PGDH1 antibody, PHOAR1 antibody, SDR36C1 antibody, MGC80546 antibody, MGC79454 antibody, AV026552 antibody, carbonyl reductase 1 antibody, 15-hydroxyprostaglandin dehydrogenase antibody, hydroxyprostaglandin dehydrogenase 15-(NAD) antibody, 15-hydroxyprostaglandin dehydrogenase L homeolog antibody, hydroxyprostaglandin dehydrogenase 15 (NAD) antibody, CBR1 antibody, HPGD antibody, hpgd.L antibody, hpgd antibody, pgdh antibody, Hpgd antibody, PTRG_03214 antibody, VDBG_09957 antibody
Background
This gene encodes a member of the short-chain nonmetalloenzyme alcohol dehydrogenase protein family. The encoded enzyme is responsible for the metabolism of prostaglandins, which function in a variety of physiologic and cellular processes such as inflammation. Mutations in this gene result in primary autosomal recessive hypertrophic osteoarthropathy and cranioosteoarthropathy. Multiple transcript variants encoding different isoforms have been found for this gene.
UniProt
Q8VCC1
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