Catalog No.
PHC92301
Species reactivity
Human, Mouse, Rat
Host species
Rabbit
Isotype
IgG
Clonality
Polyclonal
Immunogen
E. coli - derived recombinant Human COL6A2 (Phe671-Cys1019).
Tested applications
ELISA: 1:4000-1:8000, IHC: 1:50-1:100, WB: 1:1000-1:4000
Target
COL6A2, Collagen alpha-2(VI) chain
Purification
Purified by antigen affinity column.
Accession
P12110
Applications
ELISA, IHC, WB
Form
Liquid
Storage buffer
0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300.
Stability and Storage
Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Elucidating the Predominant Role of AEBP1 in Different Types of Cancers with a Focus on Glioblastoma Progression - A Review., PMID:40375702
The UCMD-Causing COL6A1 (c.930 + 189C > T) Intron Mutation Leads to the Secretion and Aggregation of Single Mutated Collagen VI α1 Chains., PMID:40225172
Involvement of muscle satellite cell dysfunction in neuromuscular disorders: Expanding the portfolio of satellite cell-opathies., PMID:35302338
Authentication of collagen VI antibodies., PMID:28755659
Collagen VI-NG2 axis in human tendon fibroblasts under conditions mimicking injury response., PMID:26944560
Expression of collagen VI α5 and α6 chains in human muscle and in Duchenne muscular dystrophy-related muscle fibrosis., PMID:22226732
Expression of the collagen VI α5 and α6 chains in normal human skin and in skin of patients with collagen VI-related myopathies., PMID:20882040
Identification and characterization of novel collagen VI non-canonical splicing mutations causing Ullrich congenital muscular dystrophy., PMID:19309692
A refined diagnostic algorithm for Bethlem myopathy., PMID:18378883
The congenital muscular dystrophies: recent advances and molecular insights., PMID:17163796
Mutations in COL6A3 cause severe and mild phenotypes of Ullrich congenital muscular dystrophy., PMID:11992252
For research use only. Not for human or drug use.
