Elabscience

COMP Polyclonal Antibody

Product Code:
 
E-AB-14886
Product Group:
 
Primary Antibodies
Supplier:
 
Elabscience
Host Type:
 
Rabbit
Antibody Isotype:
 
IgG
Antibody Clonality:
 
Polyclonal
Regulatory Status:
 
RUO
Target Species:
  • Human
  • Mouse
  • Rat
Applications:
  • Enzyme-Linked Immunosorbent Assay (ELISA)
  • Immunohistochemistry (IHC)
Shipping:
 
Ice packs
Storage:
 
-20°C
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Immunohistochemistry of paraffin-embedded Human thyroid cancer tissue using COMP Polyclonal Antibody at dilution 1:50
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Immunohistochemistry of paraffin-embedded Human breast cancer tissue using COMP Polyclonal Antibody at dilution 1:50
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Immunohistochemistry of paraffin-embedded Human thyroid cancer tissue using COMP Polyclonal Antibody at dilution 1:50
Immunohistochemistry of paraffin-embedded Human breast cancer tissue using COMP Polyclonal Antibody at dilution 1:50

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CodeSizePrice
E-AB-14886-20uL20uL£125.00
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E-AB-14886-60uL60uL£172.00
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E-AB-14886-120uL120uL£237.00
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E-AB-14886-200uL200uL£344.00
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This product comes from: China.
Typical lead time: 14-21 working days.
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Further Information

Abbreviation:
COMP
Background:
The protein encoded by this gene is a noncollagenous extracellular matrix (ECM) protein. It consists of five identical glycoprotein subunits, each with EGF-like and calcium-binding (thrombospondin-like) domains. Oligomerization results from formation of a five-stranded coiled coil and disulfides. Binding to other ECM proteins such as collagen appears to depend on divalent cations. Mutations can cause the osteochondrodysplasias pseudochondroplasia (PSACH) and multiple epiphyseal dysplasia (MED).
Buffer:
PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Concentration:
0.3 mg/mL
Conjugation:
Unconjugated
Dilution:
IHC 1:100-1:300
Immunogen:
Recombinant protein of human COMP
Purification method:
Affinity purification
Target Synonym:
cartilage oligomeric matrix protein (pseudoachondroplasia;epiphyseal dysplasia 1;multiple);Cartilage oligomeric matrix protein;Cartilage oligomeric matrix protein precursor;COMP;COMP;EDM 1;EDM1;EPD 1;EPD1;Epiphyseal dysplasia 1;Epiphyseal dysplasia 1 multiple;Epiphyseal dysplasia multiple 1;MED;MGC13181;MGC149768;PSACH;pseudoachondroplasia (epiphyseal dysplasia 1;multiple);Pseudoachondroplasia;THBS 5;THBS5;Thrombospondin 5;Thrombospondin-5;Thrombospondin5;TSP5
UNIProt ID:
P49747

Documents