MEGF11 anticorps (AA 801-900)
Aperçu rapide pour MEGF11 anticorps (AA 801-900) (ABIN6944064)
Antigène
Voir toutes MEGF11 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 801-900
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Réactivité croisée
- Souris
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Homologie
- Human,Rat,Dog,Cow,Sheep,Pig,Horse,Chicken,Rabbit,Zebrafish
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Purification
- Purified by Protein A.
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Immunogène
- KLH conjugated synthetic peptide derived from human MEGF11
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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
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Concentration
- 1 μg/μL
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Buffer
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
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Stockage commentaire
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
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Date de péremption
- 12 months
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- MEGF11 (Multiple EGF-Like-Domains 11 (MEGF11))
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Autre désignation
- MEGF11
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Sujet
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Synonyms: KIAA1781, MEG11_HUMAN, Megf11, Multiple EGF-like domains protein 11, multiple EGF-like-domains 11, Multiple epidermal growth factor-like domains 11, Multiple epidermal growth factor-like domains protein 11.
Background: MEGF11 is a 1,044 amino acid single-pass type I membrane protein that belongs to the MEGF family. MEGF11 exists as a homopolymer that primarily localizes to protruding lamellipodia in an irregular, mosaic-like adhesion pattern. Expressed at high levels in adult and fetal brain and adult spinal cord, MEGF11 is found at lower levels in kidney, ovary and heart. MEGF11 contains fourteen EGF-like domains, one EMI domain, and undergoes alternative splicing events to produce four isoforms. The gene encoding MEGF11 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
- 84465
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UniProt
- A6BM72
Antigène
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