Home > Product > Antibody > Rabbit Anti-EGF antibody
Beta urogastrone; EGF; Egf; EGF_HUMAN; Epidermal Growth Factor; Epidermal Growth Factor; HOMG4; OTTHUMP00000219721; OTTHUMP00000219722; Pro epidermal growth factor; URG; Urogastrone.
Cat:
SL4568R
Species Reactivity:
Mouse,(predicted: Rat,)
Immunogen:
KLH conjugated synthetic peptide derived from mouse EGF:1-53/53 (977-1029/1217)
Format:
Liquid
Storage instructions:
Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Concentration:
1mg/ml
Clonality:
Polyclonal
Isotype:
IgG
Applications:
WB=1:500-2000ELISA=1:5000-10000IHC-P=1:100-500IHC-F=1:100-500IF=1:50-200IEM=1:20-200ICA=1:20-200ChIP=1:20-200(Paraffin sections need to do antigen repair)not yet tested in other applications.optimal dilutions/concentrations should be determined by the end
Host:
Rabbit
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Unit:
Price: $
Product PDFs
Datasheet:


Epidermal growth factor (EGF) is an acid- and heat-stable 53 amino acid protein originally found in rodents and humans. It has been shown to be a potent mitogen for a variety of cell types both in vivo and in vitro. EGF binds to the EGF receptor on the surface of cells and mediates intrinsic phosphorylation of the receptor on tyrosine residues. It has been detected in nearly all body fluids, such as urine (urogastrone), saliva, milk and platelet-rich plasma. EGF, TGF?and vaccinia virus growth factor exhibit 30-40% amino acid homology. Several additional members of the EGF/TGF family have been described; these include Cripto, Amphiregulin and the heparin-binding EGF-like growth factor. Amphiregulin and the heparin-binding EGF-like growth factor both bind to the EGF receptor.

Subcellular Location:
Membrane.

Tissue Specificity:
Expressed in kidney, salivary gland, cerebrum and prostate.

SWISS:
P01132

Gene ID:
13645

Database links:

Entrez Gene: 13645 Mouse

Entrez Gene: 1950 Human

Omim: 131530 Human

SwissProt: P01133 Human

SwissProt: P01132 Mouse

Unigene: 419815 Human

Unigene: 252481 Mouse



Tissue Specificity : Expressed in kidney, salivary gland, cerebrum and prostate. Involvement in disease:Defects in EGF are the cause of hypomagnesemia type 4 (HOMG4); also known as renal hypomagnesemia normocalciuric. HOMG4 is a disorder characterized by massive renal hypomagnesemia and normal levels of serum calcium and calcium excretion. Clinical features include seizures, mild-to mederate psychomotor retardation, and brisk tendon reflexes.
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