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ERAB (E135) polyclonal antibody

CAT: 0013-GTR18041481-02Size: 50 μLDry Ice: NoHazardous: No
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CAT#:0013-GTR18041481-02Size:50 μL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Rabbit polyclonal antibody to ERAB (E135)
Product Name Alternative
3-hydroxyacyl-CoA dehydrogenase type-2; 17-beta-hydroxysteroid dehydrogenase 10; 17-beta-HSD 10; 3-hydroxy-2-methylbutyryl-CoA dehydrogenase; 3-hydroxyacyl-CoA dehydrogenase type II; Endoplasmic reticulum-associated amyloid beta-peptide-binding protein; Mitochondrial ribonuclease P protein 2; Mitochondrial RNase P protein 2; Short-chain type dehydrogenase/reductase XH98G2; Type II HADH; HSD17B10; ERAB; HADH2; MRPP2; SCHAD; XH98G2
UniProt
Q99714
Reactivity
Human, Mouse, Rat
Immunogen
Synthetic peptide, corresponding to amino acids 102-150 of Human ERAB.
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Metabolism Research
Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE) .
Concentration
1mg/ml
Dilution
WB: 1:500-1:1000, IHC-P: 1:50-1:200
Form
Rabbit IgG, 1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH 7.2
Molecular Weight
~ 27 kDa
Storage Conditions
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Notes
For research use only.
Tested Applications
IHC, WB
Host or Source
Rabbit
Preservative
Rabbit IgG, 1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH 7.2

UniProtKB · Q99714

3-hydroxyacyl-CoA dehydrogenase type-2

HCD2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q99714
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
HSD17B10
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
1.1.1.35
Processing
—
Secondary accessions
Q5H927, Q6IBS9, Q8TCV9, Q96HD5
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

PTM

Acetylation

Coding sequence diversity

Alternative splicing

Disease

Disease variantIntellectual disabilityNeurodegeneration

Biological process

Fatty acid metabolismLipid metabolismSteroid metabolismtRNA processing

Cellular component

MitochondrionMitochondrion nucleoid

Ligand

NAD

Molecular function

Oxidoreductase

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