Human C-Type Lectin Domain Family 4 Member K (CD207) Protein

Este producto es parte de CD207 - CD207 molecule
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546€ (100 µg)

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935106861
info@markelab.com
name
Human C-Type Lectin Domain Family 4 Member K (CD207) Protein
category
Proteins and Peptides
provider
Abbexa
reference
abx620629
tested applications
ELISA, WB, SDS-PAGE

Description

Human C-Type Lectin Domain Family 4 Member K (CD207) Protein is a recombinant Human protein produced in a Mammalian cell expression system.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Proteins and Peptides
Immunogen Target
C-Type Lectin Domain Family 4 Member K (CD207)
Host
Mammalian cells
Origin
Human
Observed MW
Molecular Weight: Calculated MW: 33.14 kDa
Sequence Fragment: Pro65-Pro328
Tag: C-terminal His tag
Expression
Recombinant
Purity
> 90% (SDS-PAGE)
Size 1
100 µg
Size 2
1 mg
Form
Lyophilized Reconstitute in sterile water to produce a stock solution.
Tested Applications
ELISA, WB, SDS-PAGE
Buffer
Prior to lyophilization: PBS pH 7.4, 1 mM EDTA, 4% Trehalose, 1% Mannitol.
Availability
Shipped within 5-12 working days.
Storage
Store at 2-8 °C if the entire vial will be used within 1 week. Aliquot and store at -20 °C for long-term storage. Avoid repeated freeze-thaw cycles.
Dry Ice
No
UniProt ID
Q9UJ71
Alias
C-type lectin domain family 4 member K,CLEC4K,Langerin
Background
Protein CD207
Note
This product is for research use only. This product is shipped with ice packs.   Not for human consumption, cosmetic, therapeutic or diagnostic use.

Descripción

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CD207 Antibody is a Rabbit Polyclonal antibody against CD207. The protein encoded by this gene is expressed only in Langerhans cells which are immature dendritic cells of the epidermis and mucosa. It is localized in the Birbeck granules, organelles present in the cytoplasm of Langerhans cells and consisting of superimposed and zippered membranes. It is a C-type lectin with mannose binding specificity, and it has been proposed that mannose binding by this protein leads to internalization of antigen into Birbeck granules and providing access to a nonclassical antigen-processing pathway. Mutations in this gene result in Birbeck granules deficiency or loss of sugar binding activity.

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