HSD17B13 anticorps (AA 59-300) (APC)
Aperçu rapide pour HSD17B13 anticorps (AA 59-300) (APC) (ABIN7998781)
Antigène
Voir toutes HSD17B13 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 59-300
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Fonction
- Anti-HSD17B13 Antibody APC Conjugated
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Réactivité croisée (Details)
- No cross reactivity with other proteins.
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Homologie
- Human HSD17B13 shares 82.6%,80.6% amino acid (aa) sequence identity with mouse,rat HSD17B13,respectively.
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Purification
- Immunogen affinity purified.
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Immunogène
- E.coli-derived human HSD17B13 recombinant protein (Position: R59-K300). Human HSD17B13 shares 82.6% and 80.6% amino acid (aa) sequence identity with mouse and rat HSD17B13, respectively.
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Isotype
- IgG
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Indications d'application
- Flow Cytometry, Optimal dilutions should be determined by end users.
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Restrictions
- For Research Use only
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Format
- Liquid
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Buffer
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- -20 °C
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Stockage commentaire
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
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Date de péremption
- 12 months
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- HSD17B13 (Hydroxysteroid (17-Beta) Dehydrogenase 13 (HSD17B13))
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Autre désignation
- HSD17B13
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Sujet
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Background: 17β-Hydroxysteroid dehydrogenase type 13 also known as 17β-HSD type 13 is an enzyme that in humans is encoded by the HSD17B13 gene. Hydroxysteroid (17-beta) dehydrogenase 13, also designated Short-chain dehydrogenase/reductase 9 (SCDR9), which regulate the availability of steroids within various tissues throughout the body. HSD17B13 is a 300 amino acid secreted protein that is highly expressed in liver and is also detected in ovary, bone marrow, kidney, brain, lung, skeletal muscle, bladder and testis. The gene encoding HSD17B13 maps to chromosome 4, which houses nearly 6 % of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
Gene Full Name: hydroxysteroid 17-beta dehydrogenase 13
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ID gène
- 345275
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UniProt
- Q7Z5P4
Antigène
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