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FBLN4 antibody (AA 26-250)

This Rabbit Polyclonal antibody specifically detects FBLN4 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN6139957

Quick Overview for FBLN4 antibody (AA 26-250) (ABIN6139957)

Target

See all FBLN4 Antibodies
FBLN4 (Fibulin 4 (FBLN4))

Reactivity

  • 56
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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This FBLN4 antibody is un-conjugated

Application

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Western Blotting (WB)
  • Binding Specificity

    • 15
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    AA 26-250

    Sequence

    SPQDSEEPDS YTECTDGYEW DPDSQHCRDV NECLTIPEAC KGEMKCINHY GGYLCLPRSA AVINDLHGEG PPPPVPPAQH PNPCPPGYEP DDQDSCVDVD ECAQALHDCR PSQDCHNLPG SYQCTCPDGY RKIGPECVDI DECRYRYCQH RCVNLPGSFR CQCEPGFQLG PNNRSCVDVN ECDMGAPCEQ RCFNSYGTFL CRCHQGYELH RDGFSCSDID ECSYS

    Cross-Reactivity

    Human

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 26-250 of human EFEMP2 (NP_058634.4).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:1000

    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

    FBLN4 (Fibulin 4 (FBLN4))

    Alternative Name

    EFEMP2

    Background

    A large number of extracellular matrix proteins have been found to contain variations of the epidermal growth factor (EGF) domain and have been implicated in functions as diverse as blood coagulation, activation of complement and determination of cell fate during development. The protein encoded by this gene contains four EGF2 domains and six calcium-binding EGF2 domains. This gene is necessary for elastic fiber formation and connective tissue development. Defects in this gene are cause of an autosomal recessive cutis laxa syndrome. Alternatively spliced transcript variants have been identified for this gene.,EFEMP2,ARCL1B,FBLN4,MBP1,UPH1,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Extracellular Matrix,EFEMP2

    Molecular Weight

    49 kDa

    Gene ID

    30008

    UniProt

    O95967
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