CMTM5 Antibody (Center)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application ![]()
| WB, E |
---|---|
Primary Accession | Q96DZ9 |
Other Accession | NP_612469.1, NP_001032365.1 |
Reactivity | Human |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | Rabbit IgG |
Calculated MW | 24653 Da |
Antigen Region | 62-88 aa |
Gene ID | 116173 |
---|---|
Other Names | CKLF-like MARVEL transmembrane domain-containing protein 5, Chemokine-like factor superfamily member 5, CMTM5, CKLFSF5 |
Target/Specificity | This CMTM5 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 62-88 amino acids from the Central region of human CMTM5. |
Dilution | WB~~1:1000 |
Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | CMTM5 Antibody (Center) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | CMTM5 |
---|---|
Synonyms | CKLFSF5 |
Cellular Location | Membrane; Multi-pass membrane protein. |
Tissue Location | Highly expressed in the brain. |

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Provided below are standard protocols that you may find useful for product applications.
Background
This gene belongs to the chemokine-like factor gene superfamily. This family of genes encodes multi-pass membrane proteins that are similar to both the chemokine and the transmembrane 4 superfamilies of signaling molecules. Alternate transcriptional splice variants of this gene, encoding different isoforms, have been characterized.
References
Li, H., et al. BMB Rep 43(3):182-187(2010)
Guo, X., et al. Biochem. Biophys. Res. Commun. 387(1):139-142(2009)
Shao, L., et al. Biochem. Biophys. Res. Commun. 379(4):866-871(2009)
Shao, L., et al. Clin. Cancer Res. 13(19):5756-5762(2007)
Lamesch, P., et al. Genomics 89(3):307-315(2007)

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