Anti-COLEC11 Antibody

$99.00$319.00

Reactivity: Human,Rat
Applications: ELISA,WB,IHC
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-COLEC11 Antibody (CSB-PA861154ESR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Collectin kidney protein 1 Antibody,CL-K1 Antibody,COLEC11 Antibody

More alternative names for the antibody
CL K1 antibody|CL K1 I antibody|CL K1 II antibody|CL K1 IIa antibody|CL K1 IIb antibody|CL-K1 antibody|CLK1 antibody|COL11_HUMAN antibody|COLEC 11 antibody|COLEC11 antibody|Collectin 11 antibody|Collectin kidney I antibody|Collectin kidney protein 1 antibody|Collectin sub family member 11 antibody|Collectin-11 antibody|Collectin11 antibody|DKFZp686N1868 antibody|MGC129470 antibody|MGC129471 antibody|MGC3279 antibody
Anti-COLEC11 antibody (ab91483)
Close sc-242495|sc-242497|

Recommended applications: ELISA, WB, IHC

Recommended dilution: Recommended dilution:WB:1:500-2000,IHC:1:20-1:200

Recommended protocols: check protocols

Name

Anti-COLEC11 Antibody

Catalogue No.

CSB-PA861154ESR2HU

Reactivity

Human, Rat

Immunogen

Recombinant human Collectin-11 protein (26-271AA)

Host

Rabbit

Applications

ELISA, WB, IHC

Recommended dilution

Recommended dilution:WB:1:500-2000,IHC:1:20-1:200

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

28 kDa

Purification

Antigen Affinity Purified

Storage

Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.

Database links

Entrez Gene:78989( Human), Omim:612502( Human), SwissProt:Q9BWP8( Human), Unigene:32603( Human), Unigene:735715( Human)

Protein function

Lectin that binds to various sugars including fucose and mannose. Has a higher affinity for fucose compared to mannose. Does not bind to glucose, N-acetylglucosamine and N-acetylgalactosamine. Also binds lipopolysaccharides (LPS). Involved in fundamental development serving as a guidance cue for neural crest cell migration (By similarity). .

Protein tissue specificity

Ubiquitous. .

Involvement in disease

3MC syndrome 2 (3MC2) [MIM:265050]: A disorder characterized by facial dysmorphism that includes hypertelorism, blepharophimosis, blepharoptosis and highly arched eyebrows, cleft lip and/or palate, craniosynostosis, learning disability and genital, limb and vesicorenal anomalies. The term 3MC syndrome includes Carnevale, Mingarelli, Malpuech, and Michels syndromes. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the COLEC10/COLEC11 family.

Protein cellular localization

Secreted .

Research area

All research areas>Signaling Intermediates>COLEC
(View all antibody categories related to Signaling Intermediates)

Note

AntibodyPlus provides antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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