Fibromodulin anticorps (AA 19-376)

N° du produit ABIN6140716

Détail du produit anti-Fibromodulin anticorps

Antigène: Fibromodulin (FMOD)

Épitope: AA 19-376

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Fibromodulin est non-conjugé

Application: Western Blotting (WB)

Séquence: QYEDDPHWWF HYLRSQQSTY YDPYDPYPYE TYEPYPYGVD EGPAYTYGSP SPPDPRDCPQ ECDCPPNFPT AMYCDNRNLK YLPFVPSRMK YVYFQNNQIT SIQEGVFDNA TGLLWIALHG NQITSDKVGR KVFSKLRHLE RLYLDHNNLT RMPGPLPRSL RELHLDHNQI SRVPNNALEG LENLTALYLQ HNEIQEVGSS MRGLRSLILL DLSYNHLRKV PDGLPSALEQ LYMEHNNVYT VPDSYFRGAP KLLYVRLSHN SLTNNGLASN TFNSSSLLEL DLSYNQLQKI PPVNTNLENL YLQGNRINEF SISSFCTVVD VVNFSKLQVL RLDGNEIKRS AMPADAPLCL RLASLIEI

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 19-376 of human FMOD (NP_002014.2).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Commentaires:

HIGH QUALITY

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur Fibromodulin

Antigène: Fibromodulin (FMOD)

Autre désignation: FMOD (FMOD Produits)

Synonymes: anticorps FMOD, anticorps AI131919, anticorps AU041740, anticorps SLRR2E, anticorps LOC100286414, anticorps sc:d0415, anticorps si:dkey-31j12.4, anticorps LOC100229381, anticorps FM, anticorps fibromodulin, anticorps fibromodulin b, anticorps FMOD, anticorps Fmod, anticorps LOC100286414, anticorps fmodb

Sujet: Fibromodulin belongs to the family of small interstitial proteoglycans. The encoded protein possesses a central region containing leucine-rich repeats with 4 keratan sulfate chains, flanked by terminal domains containing disulphide bonds. Owing to the interaction with type I and type II collagen fibrils and in vitro inhibition of fibrillogenesis, the encoded protein may play a role in the assembly of extracellular matrix. It may also regulate TGF-beta activities by sequestering TGF-beta into the extracellular matrix. Sequence variations in this gene may be associated with the pathogenesis of high myopia. Alternative splicing results in multiple transcript variants.,FMOD,FM,SLRR2E,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Extracellular Matrix,Stem Cells,Mesenchymal Stem Cells,FMOD

Poids moléculaire: 43 kDa

ID gène: 2331

UniProt: Q06828

Pathways: Glycosaminoglycan Metabolic Process