Product Name	Recombinant Rabbit Anti-COL2A1 Monoclonal Antibody
Cat No.	SLA1056M
Chinese Name	Ⅱ型胶原α1蛋白/软骨钙素重组兔单抗
Alias	ACG2; ANFH; ANFH1; AOM; COL11A3; EDMMD; LCPD; OSCDP; PLSDT; SEDC; SEDSTN; SEMDSTWK; SMDALG; STL1; VPED; Col2; Col2a; Col2a-1; Del1; Dmm; Lpk; M100413; Rgsc413; Rgsc856; CG2A1A; COLLII; CO2A1_HUMAN; COL2A1; Alpha-1 type II collagen; CO2A1_MOUSE; CO2A1_RAT; collagen type II alpha 1 chain; collagen, type II, alpha 1 (primary osteoarthritis, spondyloepiphyseal dysplasia, congenital); arthroophthalmopathy, progressive (Stickler syndrome); collagen, type II, alpha 1; collagen type II alpha 1
Host Species	Rabbit
Isotype	IgG
Clonality	Monoclonal
React Species	Human
Applications	WB (1:1000-5000) IHC-P (1:100-500) IHC-F (1:100-500) IF (1:100-500) ELISA (1:5000-20000) Not yet tested in other applications. Optimal working dilutions must be determined by the end user.
Immunogen	Recombinant human COL2A1 protein
Concentration	1mg/ml
Predicted MW.	142 kDa
Subcellular Location	Extracellular
Gene ID	1280
Swiss-Prot	P02458
Storage	0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
Background	This gene encodes the alpha-1 chain of type II collagen, a fibrillar collagen found in cartilage and the vitreous humor of the eye. Mutations in this gene are associated with achondrogenesis, chondrodysplasia, early onset familial osteoarthritis, SED congenita, Langer-Saldino achondrogenesis, Kniest dysplasia, Stickler syndrome type I, and spondyloepimetaphyseal dysplasia Strudwick type. In addition, defects in processing chondrocalcin, a calcium binding protein that is the C-propeptide of this collagen molecule, are also associated with chondrodysplasia. There are two transcripts identified for this gene. [provided by RefSeq, Jul 2008]
Attention	This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

 

FOR RESEARCH USE ONLY. Not for use in diagnostic or therapeutic procedures.