FBLN4 Protein (AA 1-229) (GST tag)

Catalog No. ABIN2752779

This Recombinant FBLN4 protein is produced in Wheat germ.

Quick Overview for FBLN4 Protein (AA 1-229) (GST tag) (ABIN2752779)

Target: FBLN4 (Fibulin 4 (FBLN4))

Protein Type: Recombinant

Origin: Human

Source: Wheat germ

Application: Western Blotting (WB), ELISA, Affinity Purification (AP), Antibody Array (AA)

Product Details

Protein Characteristics: AA 1-229

Purification tag / Conjugate: This FBLN4 protein is labelled with GST tag.

Purpose: EFEMP2 (Human) Recombinant Protein (P01)

Sequence: MGAPCEQRCF NSYGTFLCRC HQGYELHRDG FSCSDIDECS YSSYLCQYRC VNEPGRFSCH CPQGYQLLAT RLCQDIDECE SGAHQCSEAQ TCVNFHGGYR CVDTNRCVEP YIQVSENRCL CPASNPLCRE QPSSIVHRYM TITSERSVPA DVFQIQATSV YPGAYNAFQI RAGPRPAGDG PPGVRAGPGD GHHEFPHELP GQLCTEAHRL CRGLHLLRSR REPPSLHLP

Characteristics: Human EFEMP2 full-length ORF (no protein_acc, 1 a.a. - 229 a.a.) recombinant protein with GST tag at N-terminal.

Purification: in vitro wheat germ expression system

Application Details

Application Notes: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Handling

Buffer: 50 mM Tris-HCI, 10 mM reduced Glutathione, pH =8.0 in the elution buffer.

Handling Advice: Aliquot to avoid repeated freezing and thawing.

Storage: -80 °C

Storage Comment: Best use within three months from the date of receipt of this protein.

Target Details

Target: FBLN4 (Fibulin 4 (FBLN4))

Alternative Name: EFEMP2

Background: Synonyms: FBLN4,MBP1,UPH1
Gene Description: EGF-containing fibulin-like extracellular matrix protein 2
Gene Name: EFEMP2
Gene Summary: 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.
GenBank: AK098186.1

Molecular Weight: 52 kDa (theoreatical)

Gene ID: 30008