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The antibody against RCN2 was raised in rabbit using the Recombinant Human Reticulocalbin-2 protein (23-180AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.
The antibody against RCN2 was raised in rabbit using the Recombinant Human Reticulocalbin-2 protein (23-180AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.
$299.00
| Cat.No | ADC-16826A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | RCN2 |
| Form | Liquid | Species Reactivity | Human |
| Isotype | IgG | Storage Buffer | 50% Glycerol, PBS with 0.02% sodium azide, pH7.3. |
| Purification Method | Antigen affinity purified | Conjugate | Non-conjugated |
| Application | ELISA, IHC | Storage | Upon receipt |
| Immunogen Description | Recombinant Human Reticulocalbin-2 protein (23-180AA) | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | Complete sequences for the immunogen, target protein, and peptides are available upon request. | Uniprot ID | Q14257 |
Uniprot Id
Q14257
Target Species
Human
Target Name
RCN2
Target Full Name
Reticulocalbin-2
Target Function
Not known. Binds calcium.
Target Subcellular Location
Endoplasmic reticulum lumen.
Target Protein Families
CREC family
Target Tissue Specificity
Ubiquitous.
Target Synonyms
Calcium binding protein ERC 55 ; Calcium-binding protein ERC-55; E6 binding protein; E6-binding protein; E6BP; ERC 55 ; ERC55 ; Rcn2; RCN2_HUMAN; Reticulocalbin 2 EF hand calcium binding domain (endoplasmic reticulum calcium binding protein 55kD); Reticulocalbin 2; EF hand calcium binding domain ; Reticulocalbin-2; TCBP49
Target Background
The protein encoded by this gene is a calcium-binding protein located in the lumen of the ER. The protein contains six conserved regions with similarity to a high affinity Ca(+2)-binding motif, the EF-hand. This gene maps to the same region as type 4 Bardet-Biedl syndrome, suggesting a possible causative role for this gene in the disorder. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
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