FGFR1OP2 anticorps (AA 51-150) (AbBy Fluor® 594)
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- Antigène Voir toutes FGFR1OP2 Anticorps
- FGFR1OP2 (FGFR1 Oncogene Partner 2 (FGFR1OP2))
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Épitope
- AA 51-150
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp FGFR1OP2 est conjugé à/à la AbBy Fluor® 594
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Application
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Homologie
- Human,Mouse,Rat,Dog,Horse,Rabbit
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human FGFR1OP2
- Isotype
- IgG
- Top Product
- Discover our top product FGFR1OP2 Anticorps primaire
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- Indications d'application
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Agent conservateur
- ProClin
- Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Date de péremption
- 12 months
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- Antigène
- FGFR1OP2 (FGFR1 Oncogene Partner 2 (FGFR1OP2))
- Autre désignation
- FGFR1OP2 (FGFR1OP2 Produits)
- Synonymes
- anticorps FGFR1OP2, anticorps MGC143105, anticorps DKFZp459I1618, anticorps HSPC123-like, anticorps WIT3.0, anticorps 1500031J01Rik, anticorps Wit3.0, anticorps wu:fj17h04, anticorps zgc:64126, anticorps FGFR1 oncogene partner 2, anticorps FGFR1 oncogene partner 2 S homeolog, anticorps FGFR1OP2, anticorps fgfr1op2, anticorps Fgfr1op2, anticorps fgfr1op2.S
- Sujet
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Synonyms: DKFZp564O1863, FGFR1 oncogene partner 2, HSPC123, HSPC123 like, FGOP2_HUMAN.
Background: FGFR1OP2 belongs to the SIKE family. The FGFR1OP2 (FGFR1 oncogene partner 2) gene was identified through its involvement in a fusion with the FGFR1 gene. FGFR1OP2 may be involved in the wound healing pathway. It is expressed in bone marrow, spleen and thymus. A chromosomal aberration involving FGFR1OP2 may be a cause of stem cell myeloproliferative disorder (MPD). Insertion ins(12,8)(p11,p11p22) with FGFR1. MPD is characterized by myeloid hyperplasia, eosinophilia and T cell or B cell lymphoblastic lymphoma. In general it progresses to acute myeloid leukemia. The fusion protein FGFR1OP2-FGFR1 may exhibit constitutive kinase activity and be responsible for the transforming activity.
- ID gène
- 26127
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