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CTLA4 anticorps (AA 50-78)
CTLA4
Reactivité: Humain
WB, IHC (p)
Hôte: Lapin
Polyclonal
RB23352
unconjugated
Détail du produit anti-CTLA4 anticorps
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Antigène
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CTLA4
(Cytotoxic T-Lymphocyte-Associated Protein 4 (CTLA4))
Épitope
Tous les épitopes à travers CTLA4 Anticorps.
AA 50-78
Reactivité
Toutes les réactivités sur CTLA4 Anticorps
Humain
Hôte
Toutes les hôtes sur CTLA4 Anticorps
Lapin
Clonalité
Toutes les clonalités sur CTLA4 Anticorps
Polyclonal
Conjugué
Tous les conjugués à travers CTLA4 Anticorps
Cet anticorp CTLA4 est non-conjugé
Application
Tous les applications à travers CTLA4 Anticorps.
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
Purification
This antibody is purified through a protein A column, followed by peptide affinity purification.
Immunogène
This IDDM12 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 50-78 amino acids of human IDDM12.
Clone
RB23352
Isotype
IgG
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Information d'application
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Indications d'application
WB: 1:2000. WB: 1:2000. IHC-P: 1:50~100
Restrictions
For Research Use only
Stockage
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Format
Liquid
Buffer
Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
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
4 °C,-20 °C
Stockage commentaire
Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
Date de péremption
6 months
Détails sur CTLA4
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Antigène
CTLA4
(Cytotoxic T-Lymphocyte-Associated Protein 4 (CTLA4))
Autre désignation
IDDM12 (CTLA4 Produits )
Sujet
CTLA4 is a member of the immunoglobulin superfamily and encodes a protein which transmits an inhibitory signal to T cells. The protein contains a V domain, a transmembrane domain, and a cytoplasmic tail. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. The membrane-bound isoform functions as a homodimer interconnected by a disulfide bond, while the soluble isoform functions as a monomer. Mutations in this gene have been associated with insulin-dependent diabetes mellitus, Graves disease, Hashimoto thyroiditis, celiac disease, systemic lupus erythematosus, thyroid-associated orbitopathy, and other autoimmune diseases.
Poids moléculaire
24656
ID gène
1493
NCBI Accession
NP_001032720 , NP_005205
UniProt
P16410
Pathways
Cancer Immune Checkpoints
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