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CEACAM16 Polyclonal antibody, PBS Only

CEACAM16 Polyclonal Antibody for WB, IHC, Indirect ELISA

Cat No. 32196-1-PBS

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat

Applications

WB, IHC, Indirect ELISA

Carcinoembryonic Antigen Related Cell Adhesion Molecule 16, Carcinoembryonic antigen-like 2, Carcinoembryonic antigen-related cell adhesion molecule 16, CEA Cell Adhesion Molecule 16, Tectorial Membrane Component , DFNA4B

Formulation:  PBS Only
Conjugate:  Unconjugated
Size/Concentration: 

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Quantity

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Product Information

32196-1-PBS targets CEACAM16 in WB, IHC, Indirect ELISA applications and shows reactivity with human, mouse, rat samples.

Tested Reactivity human, mouse, rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen

CatNo: Ag37542

Product name: Recombinant human CEACAM16 protein

Source: e coli.-derived, PGEX-4T

Tag: GST

Domain: 295-425 aa of BC156855

Sequence: AKNTKTLLSGSASVVVKLSAAAVATMIVPVPTKPTEGQDVTLTVQGYPKDLLVYAWYRGPASEPNRLLSQLPSGTWIAGPAHTGREVGFPNCSLLVQKLNLTDTGRYTLKTVTVQGKTETLEVELQVAPLG

Predict reactive species
Full Name carcinoembryonic antigen-related cell adhesion molecule 16
Observed Molecular Weight48 kDa
GenBank Accession NumberBC156855
Gene Symbol CEACAM16
Gene ID (NCBI) 388551
RRIDAB_3742541
Conjugate Unconjugated
FormLiquid
Purification MethodAntigen affinity Purification
UNIPROT IDQ2WEN9
Storage Buffer PBS only, pH 7.3.
Storage ConditionsStore at -80°C.

Background Information

CEACAM16 (Carcinoembryonic Antigen-Related Cell Adhesion Molecule 16) is a member of the CEA family of cell adhesion molecules. It is a critical component of the tectorial membrane in the inner ear, playing a significant role in maintaining hearing function. Mutations in the CEACAM16 gene are associated with autosomal dominant nonsyndromic hearing loss (DFNA4B), characterized by progressive high-frequency hearing impairment. Research has shown that loss or dysfunction of CEACAM16 leads to structural abnormalities in the tectorial membrane, thereby affecting hearing. The identification of CEACAM16 has provided important insights into the genetic basis of hereditary hearing loss and has implications for the diagnosis and treatment of hearing disorders.

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