SMCR7 antibody (AA 201-300) (Biotin)
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- Target See all SMCR7 Antibodies
- SMCR7 (Smith-Magenis Syndrome Chromosome Region, Candidate 7 (SMCR7))
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Binding Specificity
- AA 201-300
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Reactivity
- Mouse
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This SMCR7 antibody is conjugated to Biotin
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Application
- ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- Cross-Reactivity
- Mouse
- Predicted Reactivity
- Human,Dog,Cow,Sheep,Horse,Rabbit
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human SMCR7
- Isotype
- IgG
- Top Product
- Discover our top product SMCR7 Primary Antibody
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- Application Notes
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IHC-P 1:200-400
IHC-F 1:100-500 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Preservative
- ProClin
- Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C for 12 months.
- Expiry Date
- 12 months
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- Target
- SMCR7 (Smith-Magenis Syndrome Chromosome Region, Candidate 7 (SMCR7))
- Alternative Name
- SMCR7 (SMCR7 Products)
- Synonyms
- AI482195 antibody, Gm11 antibody, MID49 antibody, mid49 antibody, Smcr7 antibody, RGD1560728 antibody, SMCR7 antibody, im:7149098 antibody, smcr7 antibody, smcr7b antibody, zgc:152920 antibody, mitochondrial elongation factor 2 antibody, mitochondrial elongation factor 2 S homeolog antibody, Mief2 antibody, MIEF2 antibody, mief2.S antibody, mief2 antibody
- Background
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Synonyms: MGC23130, MID49, MIEF2, Mitochondrial dynamic protein MID49, Mitochondrial dynamic protein of 49 kDa, Mitochondrial elongation factor 2, Smith Magenis syndrome chromosome region candidate 7, Smith-Magenis syndrome chromosomal region candidate gene 7 protein.
Background: This gene encodes an outer mitochondrial membrane protein that functions in the regulation of mitochondrial morphology. It can directly recruit the fission mediator dynamin-related protein 1 (Drp1) to the mitochondrial surface. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2011]
- Gene ID
- 125170
- UniProt
- Q96C03
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