HSPD1 anticorps (AA 27-240)
Aperçu rapide pour HSPD1 anticorps (AA 27-240) (ABIN3021182)
Antigène
Voir toutes HSPD1 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
-
-
Épitope
- AA 27-240
-
Séquence
- AKDVKFGADA RALMLQGVDL LADAVAVTMG PKGRTVIIEQ SWGSPKVTKD GVTVAKSIDL KDKYKNIGAK LVQDVANNTN EEAGDGTTTA TVLARSIAKE GFEKISKGAN PVEIRRGVML AVDAVIAELK KQSKPVTTPE EIAQVATISA NGDKEIGNII SDAMKKVGRK GVITVKDGKT LNDELEIIEG MKFDRGYISP YFINTSKGQK CEFQ
-
Réactivité croisée
- Humain, Souris, Rat
-
Attributs du produit
- Polyclonal Antibodies
-
Purification
- Affinity purification
-
Immunogène
- Recombinant fusion protein containing a sequence corresponding to amino acids 27-240 of human HSP60/HSPD1 (NP_002147.2).
-
Isotype
- IgG
-
-
-
-
Indications d'application
- WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:100,IP,1:50 - 1:200
-
Restrictions
- For Research Use only
-
-
-
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.
-
Conseil sur la manipulation
- Avoid freeze / thaw cycles
-
Stock
- -20 °C
-
Stockage commentaire
- Store at -20°C. Avoid freeze / thaw cycles.
-
-
-
: "Gold-nanorods-siRNA nanoplex for improved photothermal therapy by gene silencing." dans: Biomaterials, Vol. 78, pp. 27-39, (2016) (PubMed).
-
: "Gold-nanorods-siRNA nanoplex for improved photothermal therapy by gene silencing." dans: Biomaterials, Vol. 78, pp. 27-39, (2016) (PubMed).
-
- HSPD1 (Heat Shock 60kDa Protein 1 (Chaperonin) (HSPD1))
-
Autre désignation
- HSPD1
-
Sujet
- This gene encodes a member of the chaperonin family. The encoded mitochondrial protein may function as a signaling molecule in the innate immune system. This protein is essential for the folding and assembly of newly imported proteins in the mitochondria. This gene is adjacent to a related family member and the region between the 2 genes functions as a bidirectional promoter. Several pseudogenes have been associated with this gene. Two transcript variants encoding the same protein have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13.,HSPD1,CPN60,GROEL,HLD4,HSP-60,HSP60,HSP65,HuCHA60,SPG13,Hsp60,Epigenetics & Nuclear Signaling,RNA Binding,Signal Transduction,Cell Biology & Developmental Biology,Apoptosis,Mitochondrial Control of Apoptosis,Endocrine & Metabolism,Mitochondrial metabolism,HSPD1
-
Poids moléculaire
- 17 kDa/61 kDa
-
ID gène
- 3329
-
UniProt
- P10809
-
Pathways
- Activation of Innate immune Response, Regulation of Leukocyte Mediated Immunity, Positive Regulation of Immune Effector Process, Production of Molecular Mediator of Immune Response, Positive Regulation of Endopeptidase Activity
Antigène
-