alpha Actinin 4 anticorps
Aperçu rapide pour alpha Actinin 4 anticorps (ABIN6940951)
Antigène
Voir toutes alpha Actinin 4 (ACTN4) AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
Clone
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Purification
- Purified by Protein A/G
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Immunogène
- Recombinant full-length human ACTN4 protein
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Isotype
- IgG
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Indications d'application
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Positive Control: Human colon or kidney tissue (IHC).
Known Application: Immunohistochemistry (Formalin-fixed) (1-2 μg/mL for 30 minutes at RT),(Staining of formalin-fixed tissues requires boiling tissue sections in 10 mM citrate buffer, pH 6.0, for 10-20 min followed by cooling at RT for 20 minutes),Optimal dilution for a specific application should be determined.
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Restrictions
- For Research Use only
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Concentration
- 200 μg/mL
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Buffer
- 10 mM PBS with 0.05 % BSA & 0.05 % 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
- 4 °C,-80 °C
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Stockage commentaire
- Antibody with azide - store at 2 to 8°C. Antibody without azide - store at -20 to -80°C. Antibody is stable for 24 months. Non-hazardous. No MSDS required.
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Date de péremption
- 24 months
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- alpha Actinin 4 (ACTN4) (Actinin, alpha 4 (ACTN4))
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Autre désignation
- ACTN4
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Sujet
- The spectrin gene family encodes a diverse group of cytoskeletal proteins that include spectrins, dystrophins and -actinins. There are four tissue-specific -actinins, namely -actinin-1, -actinin-2, -actinin-3 and -actinin-4, which are localized to muscle and non-muscle cells, including skeletal, cardiac and smooth muscle cells, as well as within the cytoskeleton. Each -actinin protein contains one Actin-binding domain, two calponin-homology domains, two EF-hand domains and four spectrin repeats, through which they function as bundling proteins that can cross-link F-Actin, thus anchoring Actin to a variety of intracellular structures. Defects in the gene encoding -actinin-4 are the cause of focal segmental glomerulosclerosis 1 (FSGS1), a common renal lesion characterized by decreasing kidney function and, ultimately, renal failure.
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Poids moléculaire
- 105kDa
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ID gène
- 81
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UniProt
- O43707
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Pathways
- Proton Transport
Antigène
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