HMBS Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)
Quick Overview for HMBS Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag) (ABIN2722851)
Target
See all HMBS ProteinsProtein Type
Origin
Source
Application
Purity
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Protein Characteristics
- Transcript Variant 1
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Purification tag / Conjugate
- This HMBS protein is labelled with Myc-DYKDDDDK Tag.
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Characteristics
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- Recombinant human HMBS (transcript variant 1) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
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Hydroxymethylbilane Synthase (HMBS) (AA 1-361) protein (GST tag)
HMBS Origin: Human Host: Wheat germ Recombinant WB, ELISA, AP, AA
Hydroxymethylbilane Synthase (HMBS) (AA 1-361) protein (His-IF2DI Tag)HMBS Origin: Human Host: Escherichia coli (E. coli) Recombinant Greater than 90 % as determined by SDS-PAGE. WB, ELISA
Hydroxymethylbilane Synthase (HMBS) (AA 1-361) protein (His tag)HMBS Origin: Human Host: Escherichia coli (E. coli) Recombinant > 95 % SDS
Hydroxymethylbilane Synthase (HMBS) (Transcript Variant 2) protein (Myc-DYKDDDDK Tag)HMBS Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
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Application Notes
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays -
Comment
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The tag is located at the C-terminal.
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Restrictions
- For Research Use only
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Concentration
- 50 μg/mL
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Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
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Storage
- -80 °C
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Storage Comment
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- HMBS (Hydroxymethylbilane Synthase (HMBS))
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Alternative Name
- Hmbs
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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.
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Molecular Weight
- 39.1 kDa
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NCBI Accession
- NP_000181
Target
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