DPPA4 anticorps (AA 51-150) (Biotin)
Aperçu rapide pour DPPA4 anticorps (AA 51-150) (Biotin) (ABIN1700266)
Antigène
Voir toutes DPPA4 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 51-150
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Homologie
- Human,Mouse,Rat
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Purification
- Purified by Protein A.
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Immunogène
- KLH conjugated synthetic peptide derived from human Dppa4
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Isotype
- IgG
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Indications d'application
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IHC-P 1:200-400
IHC-F 1:100-500 -
Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 μg/μL
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Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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Agent conservateur
- ProClin
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Précaution d'utilisation
- This product contains ProClin: 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
- Store at -20°C for 12 months.
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Date de péremption
- 12 months
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- DPPA4 (Developmental Pluripotency Associated 4 (DPPA4))
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Autre désignation
- Dppa4
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Sujet
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Synonyms: 2410091M23Rik, Developmental pluripotency associated 4, Developmental pluripotency associated protein 4, Developmental pluripotency-associated protein 4, Dppa 4, DPPA4, DPPA4_HUMAN, FLJ10713.
Background: DPPA4 (developmental pluripotency associated 4) is a 304 amino acid protein that localizes to the nucleus and is thought to be involved in the maintenance of cell pluripotentiality during embryogenesis. The gene encoding DPPA4 maps to human chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
Antigène
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