CSRP2 anticorps (AA 101-193) (FITC)
Aperçu rapide pour CSRP2 anticorps (AA 101-193) (FITC) (ABIN1709788)
Antigène
Voir toutes CSRP2 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 101-193
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Homologie
- Human,Mouse,Rat,Dog,Pig,Horse,Chicken,Rabbit
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Purification
- Purified by Protein A.
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Immunogène
- KLH conjugated synthetic peptide derived from human CSRP2
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Isotype
- IgG
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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
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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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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Date de péremption
- 12 months
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- CSRP2 (Cysteine and Glycine-Rich Protein 2 (CSRP2))
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Autre désignation
- CSRP2
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Sujet
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Synonyms: CRP 2, CRP2, CSRP2, CSRP2_HUMAN, Cysteine and glycine rich protein 2, Cysteine and glycine-rich protein 2, Cysteine rich protein 2, Cysteine-rich protein 2, LIM domain only 5 smooth muscle, LIM domain only protein 5, LMO 5, LMO-5, LMO5, SmLIM, Smooth muscle cell LIM protein.
Background: CRP2 is a 193 amino acid nuclear protein that belongs to the CRP family of LIM domain proteins. Highly expressed in smooth muscle of aorta, CRP2 is thought to have a role in embryonic vascular system development and is downregulated following cell injury or PDGF-B exposure. CRP2 contains two LIM zinc-binding domains and is encoded by a gene that maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5 % of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
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ID gène
- 1466
Antigène
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