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ECM1 antibody (AA 150-250)

This anti-ECM1 antibody is a Rabbit Polyclonal antibody detecting ECM1 in WB and IF. Suitable for Human.
Catalog No. ABIN7267071

Quick Overview for ECM1 antibody (AA 150-250) (ABIN7267071)

Target

See all ECM1 Antibodies
ECM1 (Extracellular Matrix Protein 1 (ECM1))

Reactivity

  • 58
  • 20
  • 9
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 40
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  • 1
Rabbit

Clonality

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  • 30
Polyclonal

Conjugate

  • 43
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  • 3
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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
This ECM1 antibody is un-conjugated

Application

  • 43
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  • 19
  • 17
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  • 10
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  • 7
  • 5
  • 4
  • 3
  • 3
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Western Blotting (WB), Immunofluorescence (IF)
  • Binding Specificity

    • 6
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    AA 150-250

    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
  • Application Notes

    WB,1:500 - 1:2000,IF,1:50 - 1:200

    Restrictions

    For Research Use only
  • 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

    ECM1 (Extracellular Matrix Protein 1 (ECM1))

    Alternative Name

    ECM1

    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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