CNTN4 Rabbit pAb

Phospho-Myosin Light Chain 2-S19 Rabbit mAbPhospho-Myosin Light Chain 2-S19 Rabbit mAb

CNTN4 Rabbit pAb

$108.00$488.00

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$108.00$488.00

AXCAM; BIG-2

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SKU: A10339
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Catalog No. A10339
Product NameCNTN4 Rabbit pAb
Supplier Name ABclonal, Inc.
Brand Name Abclonal
Synonyms AXCAM; BIG-2
Summary Rabbit IgG polyclonal antibody for MGAT4B detection. Tested with WB, IHC, Direct ELISA in Human;Mouse;Rat.
Gene Name CNTN4
Gene Full Name alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B
Protein Name CNTN4
Uniprot/Swissprot ID Q8IWV2
Uniprot ID Q9UQ53
Entrez GeneID 152330
Clonality Polyclonal
Source/Host Rabbit
Applications WB
Application Details Western blot|0.25-0.5 μg/ml|Human, Mouse, Rat| Immunohistochemistry(Paraffin-embedded Section)|2-5 μg/ml|Human| Direct ELISA|0.1-0.5 μg/ml|Human|
Reactivity Human
Immunogen E.coli-derived human MGAT4B recombinant protein (Position: Q31-D548).
Purification Immunogen affinity purified.
Form Of Antibody Lyophilized
Reconstitution Adding 0.2 ml of distilled water will yield a concentration of 500 μg/ml.
Contents E.coli-derived human MGAT4B recombinant protein (Position: Q31-D548).
Conjugate Unconjugated
Stability & Storage At -20˚C for one year from date of receipt. After reconstitution, at 4˚C for one month. It can also be aliquotted and stored frozen at -20˚C for six months. Avoid repeated freezing and thawing.
Note Products will be shipped from the warehouse in Massachusetts. Promotion is running from time to time. Welcome to send a request for quote to message@sydlabs.com.
Order Offline Syd Labs, Inc. 4 Avenue E, Hopkinton, MA 01748 USA. Phone: 1-617-401-8149 Fax: 1-617-606-5019 Email: message@sydlabs.com

Description

This gene encodes a member of the contactin family of immunoglobulins. Contactins are axon-associated cell adhesion molecules that function in neuronal network formation and plasticity. The encoded protein is a glycosylphosphatidylinositol-anchored neuronal membrane protein that may play a role in the formation of axon connections in the developing nervous system. Deletion or mutation of this gene may play a role in 3p deletion syndrome and autism spectrum disorders. Alternative splicing results in multiple transcript variants.

Additional information

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USA

Size

20 ul, 100 ul, 200 ul, 50 ul

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