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DHDDS Rabbit Polyclonal Antibody (HRP)

CAT: 0013-GTR18371946Size: 100 µLDry Ice: NoHazardous: No
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CAT#:0013-GTR18371946Size:100 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
DHDDS Rabbit Polyclonal Antibody (HRP)
Product Name Alternative
DS, CIT, CPT, HDS, RP59, hCIT, DEDSM
UniProt
Q86SQ9
Immunogen
The immunogen is a synthetic peptide directed towards the N terminal region of human DHDDS
Clonality
Polyclonal
Conjugation
HRP
Sequence
Synthetic peptide located within the following region: NRRYAKKCQVERQEGHSQGFNKLAETLRWCLNLGILEVTVYAFSIENFKR
Field of Research
Metabolism Research
Purification
Affinity Purified
Form
Liquid. Purified antibody is supplied in high phosphate PBS, 100 mm phosphate, 150 mM NaCl, pH 7.6.
Molecular Weight
39kDa
Storage Conditions
All conjugated antibodies should be stored in light-protected vials or covered with a light protecting material (i.e. aluminum foil) . Conjugated antibodies are stable for at least 12 months at 4C. If longer storage is desired (24 months), conjugates may be diluted with up to 50% glycerol and stored at -2°C to -8°C. Freezing and thawing conjugated antibodies will compromise enzyme activity as well as antibody binding.
Notes
For research use only.
Prediction Reactivity
Bovine, Canine, Equine, Guinea pig, Human, Mouse, Rabbit, Rat, Zebrafish
Tested Applications
WB
NCBI Accession Number
NP_079163
Host or Source
Rabbit
Preservative
Liquid. Purified antibody is supplied in high phosphate PBS, 100 mm phosphate, 150 mM NaCl, pH 7.6.

UniProtKB · Q86SQ9

Dehydrodolichyl diphosphate synthase complex subunit DHDDS

DHDDS_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q86SQ9
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
DHDDS
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
2.5.1.87
Processing
—
Secondary accessions
B7Z4B9, B7ZB20, D3DPK7, D3DPK8, D3DPK9, E9KL43, Q5T0A4, Q8NE90, Q9BTG5, Q9BTK3, Q9H905
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Disease

Congenital disorder of glycosylationDisease variantEpilepsyIntellectual disabilityRetinitis pigmentosa

Cellular component

Endoplasmic reticulumMembrane

Biological process

Lipid metabolism

Ligand

MagnesiumMetal-binding

Molecular function

Transferase

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