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COL1A1 antibody (AA 1219-1464)

This anti-COL1A1 antibody is a Mouse Monoclonal antibody detecting COL1A1 in ELISA and FACS. Suitable for Human.
Catalog No. ABIN7193472

Quick Overview for COL1A1 antibody (AA 1219-1464) (ABIN7193472)

Target

See all COL1A1 Antibodies
COL1A1 (Collagen, Type I, alpha 1 (COL1A1))

Reactivity

  • 69
  • 33
  • 28
  • 13
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 82
  • 16
Mouse

Clonality

  • 71
  • 27
Monoclonal

Conjugate

  • 59
  • 10
  • 8
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
This COL1A1 antibody is un-conjugated

Application

  • 70
  • 56
  • 34
  • 28
  • 26
  • 7
  • 6
  • 5
  • 3
  • 1
  • 1
  • 1
  • 1
ELISA, Flow Cytometry (FACS)

Clone

7B1G12
  • Binding Specificity

    • 11
    • 9
    • 7
    • 6
    • 5
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1219-1464

    Purpose

    COL1A1 Antibody

    Purification

    Purified antibody

    Immunogen

    Purified recombinant fragment of human COL1A1 (AA: 1219-1464) expressed in E. Coli.

    Isotype

    IgG1
  • Application Notes

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % sodium azide.

    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

    4 °C,-20 °C

    Storage Comment

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Target

    COL1A1 (Collagen, Type I, alpha 1 (COL1A1))

    Alternative Name

    COL1A1

    Background

    This gene encodes the pro-alpha1 chains of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril-forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon. Mutations in this gene are associated with osteogenesis imperfecta types I-IV, Ehlers-Danlos syndrome type VIIA, Ehlers-Danlos syndrome Classical type, Caffey Disease and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for platelet-derived growth factor beta are located, are associated with a particular type of skin tumor called dermatofibrosarcoma protuberans, resulting from unregulated expression of the growth factor. Two transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene. [provided by R. Dalgleish, Feb 2008]

    Molecular Weight

    139 kDa

    Gene ID

    1277

    UniProt

    P02452

    Pathways

    Sensory Perception of Sound, Autophagy, Growth Factor Binding
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