Products for Research Use Only

HSD17B10 Antibody (N-Term)

CAT: 0013-GTR18324235-01Size: 50 µLDry Ice: NoHazardous: No
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CAT#:0013-GTR18324235-01Size:50 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Purified Rabbit Polyclonal Antibody (Pab)
Product Name Alternative
3-hydroxyacyl-CoA dehydrogenase type-2, 1.1.1.35, 17-beta-hydroxysteroid dehydrogenase 10, 17-beta-HSD 10, 1.1.1.51, 3-hydroxy-2-methylbutyryl-CoA dehydrogenase, 1.1.1.178, 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
Immunogen
This HSD17B10 antibody is generated from a rabbit immunized with a KLH conjugated synthetic peptide between 14-48 amino acids from human HSD17B10.
Target
HSD17B10
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Metabolism Research
Dilution
IF - 1:25, WB - 1:8000, FC - 1:25
Form
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
Molecular Weight
26923 Da
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
FC, IF, WB
Host or Source
Rabbit
Isotype
Rabbit IgG

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