Cell Biology Antibodies 18
Anti-RMND1 Antibody (CAB18254)
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- SKU:
- CAB18254
- Product Type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Cell Biology
Description
| Antibody Name: | Anti-RMND1 Antibody |
| Antibody SKU: | CAB18254 |
| Antibody Size: | 20uL, 50uL, 100uL |
| Application: | WB |
| Reactivity: | Human, Mouse, Rat |
| Host Species: | Rabbit |
| Immunogen: | Recombinant protein of human RMND1. |
| Application: | WB |
| Recommended Dilution: | WB 1:500 - 1:2000 |
| Reactivity: | Human, Mouse, Rat |
| Positive Samples: |
| Immunogen: | Recombinant protein of human RMND1. |
| Purification Method: | Affinity purification |
| Storage Buffer: | Store at -20°C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
| Isotype: | IgG |
| Sequence: | Email for sequence |
| Gene ID: | 55005 |
| Uniprot: | Q9NWS8 |
| Cellular Location: | |
| Calculated MW: | 51kDa |
| Observed MW: | Refer to figures |
| Synonyms: | RMD1, C6orf96, COXPD11, bA351K16, bA351K16.3, RMND1 |
| Background: | The protein encoded by this gene belongs to the evolutionary conserved sif2 family of proteins that share the DUF155 domain in common. This protein is thought to be localized in the mitochondria and involved in mitochondrial translation. Mutations in this gene are associated with combined oxidative phosphorylation deficiency-11. Alternatively spliced transcript variants have been found for this gene. |
| UniProt Protein Function: | RMND1: Belongs to the RMD1/sif2 family. 3 isoforms of the human protein are produced by alternative splicing. |
| UniProt Protein Details: | Chromosomal Location of Human Ortholog: 6q25.1 Cellular Component: mitochondrion Biological Process: translation Disease: Combined Oxidative Phosphorylation Deficiency 11 |
| NCBI Summary: | The protein encoded by this gene belongs to the evolutionary conserved sif2 family of proteins that share the DUF155 domain in common. This protein is thought to be localized in the mitochondria and involved in mitochondrial translation. Mutations in this gene are associated with combined oxidative phosphorylation deficiency-11. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2012] |
| UniProt Code: | Q9NWS8 |
| NCBI GenInfo Identifier: | 429836856 |
| NCBI Gene ID: | 55005 |
| NCBI Accession: | NP_001258866.1 |
| UniProt Secondary Accession: | Q9NWS8,Q0VDG6, Q5SZ48, Q5SZ83, Q6NSC5, Q96EN7, A8K8H4 |
| UniProt Related Accession: | Q9NWS8 |
| Molecular Weight: | |
| NCBI Full Name: | required for meiotic nuclear division protein 1 homolog isoform 2 |
| NCBI Synonym Full Names: | required for meiotic nuclear division 1 homolog (S. cerevisiae) |
| NCBI Official Symbol: | RMND1 |
| NCBI Official Synonym Symbols: | RMD1; C6orf96; COXPD11; bA351K16; bA351K16.3 |
| NCBI Protein Information: | required for meiotic nuclear division protein 1 homolog |
| UniProt Protein Name: | Required for meiotic nuclear division protein 1 homolog |
| Protein Family: | Required for meiotic nuclear division protein |
| UniProt Gene Name: | RMND1 |
| UniProt Entry Name: | RMND1_HUMAN |
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