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ECM1 antibody (AA 150-250)
ECM1
Reactivity: Human
WB, IF
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-ECM1 Antibody
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Target
See all ECM1 Antibodies
ECM1
(Extracellular Matrix Protein 1 (ECM1))
Binding Specificity
All epitopes for ECM1 antibodies
AA 150-250
Reactivity
All reactivities for ECM1 antibodies
Human
Host
All hosts for ECM1 antibodies
Rabbit
Clonality
All clonalities for ECM1 antibodies
Polyclonal
Conjugate
All conjugates for ECM1 antibodies
This ECM1 antibody is un-conjugated
Application
All applications for ECM1 antibodies
Western Blotting (WB), Immunofluorescence (IF)
Purpose
ECM1 Rabbit pAb
Sequence
PNEQKEGTPA PFGDQSHPEP ESWNAAQHCQ QDRSQGGWGH RLDGFPPGRP SPDNLNQICL PNRQHVVYGP WNLPQSSYSH LTRQGETLNF LEIGYSRCCH C
Cross-Reactivity
Human, Mouse
Characteristics
Polyclonal Antibodies
Purification
Affinity purification
Immunogen
A synthetic peptide corresponding to a sequence within amino acids 150-250 of human ECM1 (NP_001189787.1).
Isotype
IgG
Top Product
Discover our top product ECM1 Primary Antibody
Alternatives
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Application Details
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Application Notes
WB,1:500 - 1:2000,IF,1:50 - 1:200
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for ECM1
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Target
ECM1
(Extracellular Matrix Protein 1 (ECM1))
Alternative Name
ECM1 (ECM1 Products )
Synonyms
URBWD antibody, ECM antibody, EMILIN4 antibody, GPIa* antibody, MMRN antibody, AI663821 antibody, p85 antibody, extracellular matrix protein 1 antibody, multimerin 1 antibody, ECM1 antibody, MMRN1 antibody, Ecm1 antibody
Background
This gene encodes a soluble protein that is involved in endochondral bone formation, angiogenesis, and tumor biology. It also interacts with a variety of extracellular and structural proteins, contributing to the maintenance of skin integrity and homeostasis. Mutations in this gene are associated with lipoid proteinosis disorder (also known as hyalinosis cutis et mucosae or Urbach-Wiethe disease) that is characterized by generalized thickening of skin, mucosae and certain viscera. Alternatively spliced transcript variants encoding distinct isoforms have been described for this gene.,ECM1,URBWD,Immunology & Inflammation,ECM1
Molecular Weight
19kDa/46kDa/60kDa/63kDa
Gene ID
1893
UniProt
Q16610
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