Fibulin-4 Polyclonal Antibody
€0.00
In stock
SKU
ELK-ES5708
Catalog Number: ELK-ES5708
Reactivity: Human
Applications: WB, IHC-p, IF, ELISA
Information
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Reactivity: Human
Applications: WB, IHC-p, IF, ELISA
Information
Request Manual ELK-
Questions? Contact us!
Background:
EGF containing fibulin like extracellular matrix protein 2(EFEMP2) Homo sapiens 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. [provided by RefSeq, Jan 2011],
Alternative Names:
EFEMP2, FBLN4, EGF-containing fibulin-like extracellular matrix protein 2, Fibulin-4, FIBL-4, Protein UPH1
Immunogen: The antiserum was produced against synthesized peptide derived from human EFEMP2. AA range:91-140
Isotype: Rabbit
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration: 1 mg/ml
Observed band: 50
GeneID: EFEMP2
Storage: -20°C/1 year
NOTE: For Research Use Only
EGF containing fibulin like extracellular matrix protein 2(EFEMP2) Homo sapiens 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. [provided by RefSeq, Jan 2011],
Alternative Names:
EFEMP2, FBLN4, EGF-containing fibulin-like extracellular matrix protein 2, Fibulin-4, FIBL-4, Protein UPH1
Immunogen: The antiserum was produced against synthesized peptide derived from human EFEMP2. AA range:91-140
Isotype: Rabbit
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration: 1 mg/ml
Observed band: 50
GeneID: EFEMP2
Storage: -20°C/1 year
NOTE: For Research Use Only
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