Antibody data
- Antibody Data
- Antigen structure
- References [3]
- Comments [0]
- Validations [0]
Submit
Validation data
Reference
Comment
Report error
- Product number
- HPA031399 - Provider product page
- Provider
- Atlas Antibodies
- Proper citation
- Atlas Antibodies Cat#HPA031399, RRID:AB_10601156
- Product name
- Anti-RMND1
- Antibody type
- Polyclonal
- Description
- Polyclonal Antibody against Human RMND1, Gene description: required for meiotic nuclear division 1 homolog (S. cerevisiae), Alternative Gene Names: bA351K16.3, C6orf96, FLJ20627, RMD1, Validated applications: WB, IHC, Uniprot ID: Q9NWS8, Storage: Store at +4°C for short term storage. Long time storage is recommended at -20°C.
- Reactivity
- Human
- Host
- Rabbit
- Conjugate
- Unconjugated
- Isotype
- IgG
- Vial size
- 100 µl
- Concentration
- 0.1 mg/ml
- Storage
- Store at +4°C for short term storage. Long time storage is recommended at -20°C.
- Handling
- The antibody solution should be gently mixed before use.
Submitted references BRCA1-associated R-loop affects transcription and differentiation in breast luminal epithelial cells
Periventricular Calcification, Abnormal Pterins and Dry Thickened Skin: Expanding the Clinical Spectrum of RMND1?
Infantile Encephaloneuromyopathy and Defective Mitochondrial Translation Are Due to a Homozygous RMND1 Mutation
Chiang H, Zhang X, Li J, Zhao X, Chen J, Wang H, Jatoi I, Brenner A, Hu Y, Li R
Nucleic Acids Research 2019;47(10):5086-5099
Nucleic Acids Research 2019;47(10):5086-5099
Periventricular Calcification, Abnormal Pterins and Dry Thickened Skin: Expanding the Clinical Spectrum of RMND1?
Casey J, Crushell E, Thompson K, Twomey E, He L, Ennis S, Philip R, Taylor R, King M, Lynch S
2015;26
2015;26
Infantile Encephaloneuromyopathy and Defective Mitochondrial Translation Are Due to a Homozygous RMND1 Mutation
Garcia-Diaz B, Barros M, Sanna-Cherchi S, Emmanuele V, Akman H, Ferreiro-Barros C, Horvath R, Tadesse S, El Gharaby N, DiMauro S, De Vivo D, Shokr A, Hirano M, Quinzii C
The American Journal of Human Genetics 2012;91(4):729-736
The American Journal of Human Genetics 2012;91(4):729-736
No comments: Submit comment
No validations: Submit validation data