FRMD5 anticorps (AA 211-312) (Biotin)
Aperçu rapide pour FRMD5 anticorps (AA 211-312) (Biotin) (ABIN897794)
Antigène
Reactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 211-312
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Réactivité croisée
- Humain
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Homologie
- Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit
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Purification
- Purified by Protein A.
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Immunogène
- KLH conjugated synthetic peptide derived from human FRMD5
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Isotype
- IgG
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Indications d'application
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WB 1:300-5000
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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- FRMD5 (FERM Domain Containing 5 (FRMD5))
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Autre désignation
- FRMD5
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Sujet
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Synonyms: FERM domain containing 5, FERM domain-containing protein 5, FLJ41022, FRMD5, FRMD5_HUMAN, MGC14161.
Background: FERM domains are roughly 150 amino acids in length and are found in a number of cytoskeletal-associated proteins such as Ezrin, Radixin, Moesin and 4.1 (erythrocyte membrane protein band 4.1), where they provide a link between cytoskeletal signals and membrane dynamics. FRMD5 (FERM domain-containing protein 5) is a 570 amino acid single-pass membrane protein that contains one FERM domain and exists as two alternatively spliced isoforms. The gene encoding FRMD5 maps to human chromosome 15, which houses over 700 genes and comprises nearly 3 % of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
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ID gène
- 84978
Antigène
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