Mouse Anti-DDHD1 Antibody (CBMOAB-40524FYA)
Cat: CBMOAB-40524FYA
Certificate of Analysis Lookup
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Lot Number
To download a Certificate of Analysis, please enter a lot number in the search box below. Note: Certificate of Analysis not available for kit components.
Lot Number
- Product List
- Specifications
- Application Information
- Target
Sub Cat | Clonality | Species Reactivity | Application | Clone | Conjugate | Size | |
CBMOAB-40524FYA | Monoclonal | Rhesus (Macaca mulatta), Cattle (Bos taurus), Chimpanzee (Pan troglodytes), Frog (Xenopus laevis), Marmoset | WB, ELISA | MO40524FYA | 100 µg | ||
MO-AB-01855W | Monoclonal | Rhesus (Macaca mulatta) | WB, ELISA | MO01855W | 100 µg | ||
MO-AB-02912H | Monoclonal | Frog (Xenopus laevis) | WB, ELISA | MO02912C | 100 µg | ||
MO-AB-11262R | Monoclonal | Cattle (Bos taurus) | WB, ELISA | MO11262R | 100 µg | ||
MO-AB-21223W | Monoclonal | Chimpanzee (Pan troglodytes) | WB, ELISA | MO21223W | 100 µg | ||
MO-AB-54010W | Monoclonal | Marmoset | WB, ELISA | MO54010W | 100 µg |
Specifications
Host species | Mouse (Mus musculus) |
Species Reactivity | Rhesus (Macaca mulatta), Cattle (Bos taurus), Chimpanzee (Pan troglodytes), Frog (Xenopus laevis), Marmoset |
Clone | MO40524FYA |
Specificity | This antibody binds to Rhesus DDHD1. |
Format | Liquid or Lyophilized |
Storage | Store at 4°C: short-term (1-2weeks) Store at -20°C: long-term and future use |
Purity | > 90% was determined by SDS-PAGE |
Purification | Purified with Protein A or G affinity chromatography |
Application Information
Application | WB, ELISA |
Application Notes | ELISA: 1:1000-1:3000 Other applications are to be developed. The optimal dilution should be determined by the end user. |
Target
Introduction | This gene is a member of the intracellular phospholipase A1 gene family. The protein encoded by this gene preferentially hydrolyzes phosphatidic acid. It is a cytosolic protein with some mitochondrial localization, and is thought to be involved in the regulation of mitochondrial dynamics. Overexpression of this gene causes fragmentation of the tubular structures in mitochondria, while depletion of the gene results in mitochondrial tubule elongation. Deletion of this gene in male mice caused fertility defects, resulting from disruption in the organization of the mitochondria during spermiogenesis. In humans, mutations in this gene have been associated with hereditary spastic paraplegia (HSP), also known as Strumpell-Lorrain disease, or, familial spastic paraparesis (FSP). This inherited disorder is characterized by progressive weakness and spasticity of the legs. Alternative splicing results in multiple transcript variants encoding different isoforms. |
Product Overview | Mouse Anti-Rhesus DDHD1 Antibody is a mouse antibody against DDHD1. It can be used for DDHD1 detection in Western Blot, Enzyme-Linked Immunosorbent Assay. |
Alternative Names | DDHD1 |
UniProt ID | F7AJU1 |
Protein Refseq | The length of the protein is 899 amino acids long. The sequence is show below: MNYPGRGSPRSPEHNGRGGGGAWELGSDAGPAFGGGVCCFEHLPGGDPGDGDVPLALLRGDPGLHLAPGTEDHNHHLALDPCLSDENYDFSSAESGSSLRYYSEGESGGGGSSLSLHPPQQAPLVPTNSGGGGATGGVPGERKRTRLGGPAARHRYEVVTELGPEEVRWFYKEDKKTWKPFIGYDSLRIELAFRTLLQATGARRQGEDRDGDHVCSPTGPASSSGEDDDEDRACGFCQSTTGHEPEMVELVNIEPVCVRGGLYEVDVTQGECYPVYWNQADKIPVMRGQWFIDGTWQPLEEEESNLIEQEHLNCFRGQQMQENFDIEVSKSIDGKDAVHSFKLSRNHVDWHSVDEVYLYSDATTSKIARTVTQKLGFSKASSSGTRLHRGYVEEATLEDKPSQTTHIVFVVHGIGQKMDQGRIIKNTAMMREAARKIEERHFSNHATHVEFLPVEWRSKLTLDGDTVDSITPDKVRGLRDMLNSSAMDIMYYTSPLYRDELVKGLQQELNRLYSLFCSRNPDFEEKGGKVSIVSHSLGCVITYDIMTGWNPVRLYEQLLQKEEELPDERWMSYEERHLLDELYITKRRLKEIEERLHGLKASSMTQTPALKFKVENFFCMGSPLAVFLALRGIRPGNTGSQDHILPREICNRLLNIFHPTDPVAYRLEPLILKHYSNISPVQIHWYNTSNPLPYEHMKPSFLNPAKEPTSVSENEGISTIPSPVTSPVLSRRHYGESITNIGKASILGAASIGKGLGGMLFSRFGRSSTTPSSETSKDSMEDEKKPVASPSATTVATQTLPHSSSGFLDSAYFRLQESFFNLPQLLFPENVMQNKDNALVELDHRIDFELREGLVESRYWSAVTSHTAYWSSLDVALFLLTFMYKHEHDNDAKPNLDPI. |
For Research Use Only | Not For Clinical Use.
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