ADAMTS2 Recombinant antibody

ADAMTS2 Recombinant Antibody for WB, IF/ICC, ELISA
Cat No. 84476-6-RR
Clone No.241860B8

Host / Isotype

Rabbit / IgG

Reactivity

human

Applications

WB, IF/ICC, ELISA

ADAMTS-2, pNPI, PCPNI, PCINP, ADAMTS 2

Formulation:  PBS and Azide
PBS and Azide
PBS Only
Conjugate:  Unconjugated
Unconjugated
Size/Concentration: 

-/ -

Freight/Packing: -

Quantity

Please visit your regions distributor:


Tested Applications

Positive WB detected inA431 cells, COLO 205 cells, PC-3 cells, HT-1080 cells
Positive IF/ICC detected inA431 cells

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:5000-1:50000
Immunofluorescence (IF)/ICCIF/ICC : 1:125-1:500
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

84476-6-RR targets ADAMTS2 in WB, IF/ICC, ELISA applications and shows reactivity with human samples.

Tested Reactivity human
Host / Isotype Rabbit / IgG
Class Recombinant
Type Antibody
Immunogen ADAMTS2 fusion protein Ag34957 Predict reactive species
Full Name ADAM metallopeptidase with thrombospondin type 1 motif, 2
Calculated Molecular Weight135 kDa
Observed Molecular Weight110~130 kDa
GenBank Accession NumberNM_014244
Gene Symbol ADAMTS2
Gene ID (NCBI) 9509
RRIDAB_3671997
Conjugate Unconjugated
Form Liquid
Purification MethodProtein A purfication
UNIPROT IDO95450
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol , pH 7.3
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.

Background Information

A disintegrin and metalloproteinase with thrombospondin motifs 2 (ADAMTS-2) is a metalloproteinase that plays a key role in the processing of fibrillar procollagen precursors into mature collagen molecules by excising the amino-propeptide. ADAMTS-2 can, like the procollagen C-proteinases, be regulated by transforming growth factor-β1 (TGF-β1), with implications for mechanisms whereby this growth factor effects net increases in formation of extracellular matrix. Mutations in the ADAMTS-2 gene cause dermatosparaxis in human (dermatosparactic type of Ehlers-Danlos syndrome, also known as Ehlers-Danlos syndrome type VIIC). Human ADAMTS-2 has eight potential sites for Asn-linked glycosylation and other mammals (PMID: 16046392, 12646579).

Protocols

Product Specific Protocols
WB protocol for ADAMTS2 antibody 84476-6-RRDownload protocol
IF protocol for ADAMTS2 antibody 84476-6-RRDownload protocol
Standard Protocols
Click here to view our Standard Protocols
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