anti-Multiple EGF-Like-Domains 8 (MEGF8) Antibodies

The protein encoded by MEGF8 is a single-pass type I membrane protein of unknown function that contains several EGF-like domains, Kelch repeats, and PSI domains. Additionally we are shipping and many more products for this protein.

list all antibodies	Gene Name	GeneID	UniProt
	MEGF8	1954	Q7Z7M0
Anti-Mouse MEGF8	MEGF8	269878	P60882
Anti-Rat MEGF8	MEGF8	114029

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Top anti-MEGF8 Antibodies at antibodies-online.com

Showing 8 out of 11 products:

Catalog No.	Reactivity	Host	Conjugate	Application	Quantity	Supplier	Delivery	Price	Details
ABIN1535042	Human	Rabbit	Un-conjugated	ELISA, WB	100 μg	Log in to see	2 to 3 Days	$302.50	Details
ABIN3184416	Human	Rabbit	Un-conjugated	ELISA, IHC, WB	100 μL	Log in to see	16 Days	$181.73	Details
ABIN4333462	Human	Rabbit	Un-conjugated	IHC, IHC (p)	0.1 mL	Log in to see	10 to 13 Days	$491.63	Details
ABIN1455891	Human	Rabbit	Un-conjugated	ELISA, WB	100 μg	Log in to see	2 to 3 Days	$302.50	Details
ABIN2878146	Human	Rabbit	Un-conjugated	IHC, WB	100 μL	Log in to see	7 to 9 Days	$581.17	Details
ABIN866078	Human	Mouse	Un-conjugated	ICC, WB	100 μL	Log in to see	12 to 14 Days	$351.92	Details
ABIN5618235	Human	Rabbit	Un-conjugated	ELISA, WB	100 μg	Log in to see	2 to 3 Days	$447.27	Details
ABIN1577850	Human	Rabbit	Un-conjugated	ELISA, WB	100 μg	Log in to see	12 to 14 Days	$351.92	Details

MEGF8 Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes	Applications	Host	Clonality
Human	,	,	,

More Antibodies against MEGF8 Interaction Partners

Human Multiple EGF-Like-Domains 8 (MEGF8) interaction partners

mutations in MEGF8 cause a Carpenter syndrome subtype frequently associated with defective left-right patterning, probably through perturbation of signaling by hedgehog (show SHH Antibodies) and nodal family members.

Mouse (Murine) Multiple EGF-Like-Domains 8 (MEGF8) interaction partners

Megf8 attenuates signaling through the Hedgehog (show SHH Antibodies) pathway by reducing levels of Smoothened at the cell surface and the primary cilium. Mutations in Megf8 lead to cardiac defects, limb defects, left-right patterning defects and craniofacial anomalies.
Megf8 is involved in mediating BMP4 (show BMP4 Antibodies) signaling and guidance of developing trigeminal ganglia axons.

MEGF8 Antigen Profile

Protein Summary

The protein encoded by this gene is a single-pass type I membrane protein of unknown function that contains several EGF-like domains, Kelch repeats, and PSI domains. Defects in this gene are a cause of Carpenter syndrome 2. Two transcript variants encoding different isoforms have been found for this gene.

Gene names and symbols associated with MEGF8

multiple EGF like domains 8 (MEGF8) antibody
multiple EGF-like-domains 8 (Megf8) antibody

AW049492 antibody
b2b288Clo antibody
b2b1702Clo antibody
C19orf49 antibody
CRPT2 antibody
Egfl4 antibody
mKIAA0817 antibody
SBP1 antibody

Protein level used designations for MEGF8

EGF-like domain-containing protein 4 , EGF-like-domain, multiple 4 , HBV pre-s2 binding protein 1 , epidermal growth factor-like protein 4 , multiple epidermal growth factor-like domains protein 8 , EGF-like protein 4 , multiple EGF-like domains protein 8 , multiple EGF-like domain protein 4

GENE ID	SPECIES
1954	Homo sapiens
269878	Mus musculus
114029	Rattus norvegicus

Selected quality suppliers for anti-MEGF8 (MEGF8) Antibodies

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