EFR3A anticorps (AbBy Fluor® 750)
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- Antigène Voir toutes EFR3A Anticorps
- EFR3A (EFR3 Homolog A (EFR3A))
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Reactivité
- Humain, Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp EFR3A est conjugé à/à la AbBy Fluor® 750
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Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Réactivité croisée
- Humain, Souris, Rat
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human EFR3A
- Isotype
- IgG
- Top Product
- Discover our top product EFR3A Anticorps primaire
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- Indications d'application
- IF(IHC-P) 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
- EFR3A (EFR3 Homolog A (EFR3A))
- Autre désignation
- EFR3A (EFR3A Produits)
- Synonymes
- anticorps RGD1305976, anticorps A130089M23Rik, anticorps BB071175, anticorps C76891, anticorps C920006C10Rik, anticorps D030063F01Rik, anticorps mKIAA0143, anticorps EFR3 homolog A, anticorps EFR3 homolog A L homeolog, anticorps Efr3a, anticorps EFR3A, anticorps efr3a.L
- Sujet
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Synonyms: EFR 3A, EFR3 homolog A S. cerevisiae, EFR3 homolog A, KIAA0143, Protein EFR3 homolog A, Protein EFR3 like,
Background: EFR3A is a plasma membrane protein that contains 821 amino acids and belongs to the EFR3 family. EFR3A is alternatively spliced creating three isoforms and is encoded by a gene that maps to human chromosome 8. Human chromosome 8 consists of nearly 146 million base pairs, encodes over 800 genes and is associated with a variety of diseases and malignancies. Schizophrenia, bipolar disorder, Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism, Waardenburg syndrome and some leukemias and lymphomas are thought to occur as a result of defects in specific genes that map to chromosome 8.
- ID gène
- 23167
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