C1QTNF2 anticorps (AA 101-200)
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- Antigène Tous les produits C1QTNF2
- C1QTNF2 (C1q and Tumor Necrosis Factor Related Protein 2 (C1QTNF2))
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Épitope
- AA 101-200
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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 C1QTNF2 est non-conjugé
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Application
- Western Blotting (WB), ELISA, Immunocytochemistry (ICC), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- Réactivité croisée
- Humain
- Homologie
- Mouse,Rat,Cow,Pig
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human CTRP2
- Isotype
- IgG
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- Indications d'application
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- Stockage commentaire
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- Date de péremption
- 12 months
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- Antigène
- C1QTNF2 (C1q and Tumor Necrosis Factor Related Protein 2 (C1QTNF2))
- Autre désignation
- CTRP2 (C1QTNF2 Produits)
- Synonymes
- anticorps C1QTNF2, anticorps fe50b04, anticorps wu:fe50b04, anticorps CTRP2, anticorps zacrp2, anticorps 1810033K05Rik, anticorps Ctrp2, anticorps RGD1561041, anticorps C1q and tumor necrosis factor related protein 2, anticorps C1q and TNF related 2, anticorps C1QTNF2, anticorps c1qtnf2, anticorps C1qtnf2
- Sujet
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Synonyms: C1q and tumor necrosis factor related protein 2, C1QT2_HUMAN, C1qtnf2, Complement C1q tumor necrosis factor-related protein 2, CTRP2, Zacrp2.
Background: CTRP2 is a 285 amino acid secreted protein that contains one C1q domain and one collagen-like domain and is encoded by a gene that maps to human chromosome 5. Chromosome 5 contains 181 million base pairs and comprises nearly 6 % of the human genome. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5-associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome, while deletion of the q arm or of chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
- ID gène
- 114898
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