C1S anticorps (AA 479-688)

N° du produit ABIN6137765

Détail du produit anti-C1S anticorps

Antigène: C1S (Complement Component 1, S Subcomponent (C1S))

Épitope: AA 479-688

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C1S est non-conjugé

Application: Western Blotting (WB)

Séquence: GNREPTMYVG STSVQTSRLA KSKMLTPEHV FIHPGWKLLE VPEGRTNFDN DIALVRLKDP VKMGPTVSPI CLPGTSSDYN LMDGDLGLIS GWGRTEKRDR AVRLKAARLP VAPLRKCKEV KVEKPTADAE AYVFTPNMIC AGGEKGMDSC KGDSGGAFAV QDPNDKTKFY AAGLVSWGPQ CGTYGLYTRV KNYVDWIMKT MQENSTPRED

Réactivité croisée: Humain, Rat

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 479-688 of human C1S (NP_958850.1).

Isotype: IgG

Information d'application

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

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 C1S

Antigène: C1S (Complement Component 1, S Subcomponent (C1S))

Autre désignation: C1S (C1S Produits)

Synonymes: anticorps AA959438, anticorps AI255193, anticorps AI327365, anticorps C1sa, anticorps r-gsp, anticorps C1S, anticorps complement C1s, anticorps complement component 1, s subcomponent 1, anticorps complement component 1, s subcomponent, anticorps complement component 1, s subcomponent L homeolog, anticorps complement C1s subcomponent, anticorps C1S, anticorps C1s1, anticorps C1s, anticorps c1s, anticorps c1s.L, anticorps LOC100558615

Sujet: This gene encodes a serine protease, which is a major constituent of the human complement subcomponent C1. C1s associates with two other complement components C1r and C1q in order to yield the first component of the serum complement system. Defects in this gene are the cause of selective C1s deficiency.,C1S,EDSPD2,Signal Transduction,G protein signaling,G-Protein-Coupled Receptors(GPCR),Immunology & Inflammation,Cell Intrinsic Innate Immunity Signaling Pathway,C1S

Poids moléculaire: 76 kDa

ID gène: 716

UniProt: P09871

Pathways: Système du Complément