ADAMTS3 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PA551299-Each-of-1 | In Stock | ₹ 46,057.50 |
PA551299 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,057.50
GST (18%): ₹ 8,290.35
Total Price: ₹ 54,347.85
Antigen
ADAMTS3
Classification
Polyclonal
Conjugate
Unconjugated
Gene
ADAMTS3
Gene Alias
a disintegrin and metalloproteinase; A disintegrin and metalloproteinase with thrombospondin motifs 3; a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 3; ADAM; ADAM metallopeptidase with thrombospondin type 1 motif 3; ADAM metallopeptidase with thrombospondin type 1 motif, 3; ADAMs; ADAM-TS 3; ADAMTS3; ADAM-TS3; ADAMTS-3; ADAMTS-4; KIAA0366; metalloendopeptidases; PC II-NP; procollagen II amino propeptide-processing enzyme; Procollagen II N-proteinase; zinc metalloendopeptidase
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
9508
Content And Storage
-20°C
Form
Liquid
Applications
Immunohistochemistry (Paraffin)
Concentration
1.7 mg/mL
Formulation
PBS with 40% glycerol and 0.05% sodium azide; pH 7.4
Gene Accession No.
O15072
Gene Symbols
ADAMTS3
Immunogen
Synthetic peptide of human ADAMTS3
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
Description
- The antibody detects endogenous levels of total ADAMTS3 protein
- This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family
- Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif
- Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains
- The protein encoded by this gene is the major procollagen II N-propeptidase
- A deficiency of this protein may be responsible for dermatosparaxis, a genetic defect of connective tissues.