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HMBS antibody (AA 1-361)
HMBS
Reactivity: Human
WB
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-HMBS Antibody
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Target
See all HMBS Antibodies
HMBS
(Hydroxymethylbilane Synthase (HMBS))
Binding Specificity
All epitopes for HMBS antibodies
AA 1-361
Reactivity
All reactivities for HMBS antibodies
Human
Host
All hosts for HMBS antibodies
Rabbit
Clonality
All clonalities for HMBS antibodies
Polyclonal
Conjugate
All conjugates for HMBS antibodies
This HMBS antibody is un-conjugated
Application
All applications for HMBS antibodies
Western Blotting (WB)
Sequence
MSGNGNAAAT AEENSPKMRV IRVGTRKSQL ARIQTDSVVA TLKASYPGLQ FEIIAMSTTG DKILDTALSK IGEKSLFTKE LEHALEKNEV DLVVHSLKDL PTVLPPGFTI GAICKRENPH DAVVFHPKFV GKTLETLPEK SVVGTSSLRR AAQLQRKFPH LEFRSIRGNL NTRLRKLDEQ QEFSAIILAT AGLQRMGWHN RVGQILHPEE CMYAVGQGAL GVEVRAKDQD ILDLVGVLHD PETLLRCIAE RAFLRHLEGG CSVPVAVHTA MKDGQLYLTG GVWSLDGSDS IQETMQATIH VPAQHEDGPE DDPQLVGITA RNIPRGPQLA AQNLGISLAN LLLSKGAKNI LDVARQLNDA H
Cross-Reactivity
Human, Mouse
Characteristics
Polyclonal Antibodies
Purification
Affinity purification
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 1-361 of human HMBS (NP_000181.2).
Isotype
IgG
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Discover our top product HMBS Primary Antibody
Alternatives
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Application Details
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Application Notes
WB,1:500 - 1:2000
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Handling Advice
Avoid freeze / thaw cycles
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for HMBS
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Target
HMBS
(Hydroxymethylbilane Synthase (HMBS))
Alternative Name
HMBS (HMBS Products )
Background
This gene encodes a member of the hydroxymethylbilane synthase superfamily. The encoded protein is the third enzyme of the heme biosynthetic pathway and catalyzes the head to tail condensation of four porphobilinogen molecules into the linear hydroxymethylbilane. Mutations in this gene are associated with the autosomal dominant disease acute intermittent porphyria. Alternatively spliced transcript variants encoding different isoforms have been described.,HMBS,PBG-D,PBGD,PORC,UPS,HMBS
Molecular Weight
33 kDa/34 kDa/37 kDa/39 kDa
Gene ID
3145
UniProt
P08397
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