Anti CNNM4 pAb (ATL-HPA017732 w/enhanced validation)
Atlas Antibodies
- SKU:
- ATL-HPA017732-25
- Shipping:
- Calculated at Checkout
$303.00
Gene Name: CNNM4
Alternative Gene Name: ACDP4, KIAA1592
Isotype: IgG
Interspecies mouse/rat: ENSMUSG00000037408: 77%, ENSRNOG00000015886: 78%
Entrez Gene ID: 26504
Uniprot ID: Q6P4Q7
Buffer: 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative.
Storage Temperature: Store at +4°C for short term storage. Long time storage is recommended at -20°C.
Product Specifications | |
Application | IHC |
Reactivity | Human |
Clonality | Polyclonal |
Host | Rabbit |
Immunogen | FSYYGTMALTSVPSDRSPAHPTPLSRSASLSYPDRTDVSTAATLAGSSNQFGSSVLGQYISDFSVRALVDLQYIKITRQQYQNGLLASRMENSPQFPIDGCTTHMENLAEKSELPVVDETTTLLNERNSL |
Gene Sequence | FSYYGTMALTSVPSDRSPAHPTPLSRSASLSYPDRTDVSTAATLAGSSNQFGSSVLGQYISDFSVRALVDLQYIKITRQQYQNGLLASRMENSPQFPIDGCTTHMENLAEKSELPVVDETTTLLNERNSL |
Gene ID - Mouse | ENSMUSG00000037408 |
Gene ID - Rat | ENSRNOG00000015886 |
Buffer | 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative. |
Documents & Links for Anti CNNM4 pAb (ATL-HPA017732 w/enhanced validation) | |
Datasheet | Anti CNNM4 pAb (ATL-HPA017732 w/enhanced validation) Datasheet (External Link) |
Vendor Page | Anti CNNM4 pAb (ATL-HPA017732 w/enhanced validation) at Atlas Antibodies |
Documents & Links for Anti CNNM4 pAb (ATL-HPA017732 w/enhanced validation) | |
Datasheet | Anti CNNM4 pAb (ATL-HPA017732 w/enhanced validation) Datasheet (External Link) |
Vendor Page | Anti CNNM4 pAb (ATL-HPA017732 w/enhanced validation) |
Citations for Anti CNNM4 pAb (ATL-HPA017732 w/enhanced validation) – 1 Found |
Parry, David A; Mighell, Alan J; El-Sayed, Walid; Shore, Roger C; Jalili, Ismail K; Dollfus, Hélène; Bloch-Zupan, Agnes; Carlos, Roman; Carr, Ian M; Downey, Louise M; Blain, Katharine M; Mansfield, David C; Shahrabi, Mehdi; Heidari, Mansour; Aref, Parissa; Abbasi, Mohsen; Michaelides, Michel; Moore, Anthony T; Kirkham, Jennifer; Inglehearn, Chris F. Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta. American Journal Of Human Genetics. 2009;84(2):266-73. PubMed |