SMCR7 antibody (N-Term)

Catalog No. ABIN2791915

The Rabbit Polyclonal anti-SMCR7 antibody (ABIN2791915) specifically detects SMCR7 in WB. The antibody is reactive with Human, Guinea Pig, Horse and Rat samples.

Quick Overview for SMCR7 antibody (N-Term) (ABIN2791915)

Target: SMCR7 (Smith-Magenis Syndrome Chromosome Region, Candidate 7 (SMCR7))

Reactivity: Human, Guinea Pig, Horse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SMCR7 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-SMCR7 Antibody

Binding Specificity: N-Term

Sequence: FSQKRGKRRS DEGLGSMVDF LLANARLVLG VGGAAVLGIA TLAVKRFIDR

Predicted Reactivity: Guinea Pig: 79%, Horse: 86%, Human: 100%, Rat: 79%

Characteristics: This is a rabbit polyclonal antibody against SMCR7. It was validated on Western Blot.

Purification: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the N-terminal region of Human SMCR7

Application Details

Application Notes: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handling Advice: Avoid repeat freeze-thaw cycles.

Storage: -20 °C

Storage Comment: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Target Details for SMCR7

Target: SMCR7 (Smith-Magenis Syndrome Chromosome Region, Candidate 7 (SMCR7))

Alternative Name: SMCR7

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.
Alias Symbols: MID49
Protein Interaction Partner: AGTRAP, UBQLN1, RABAC1, DNM1L, UBC, UBQLN4, PSMF1,
Protein Size: 465

Molecular Weight: 50 kDa

Gene ID: 125170

NCBI Accession: NM_148886, NP_683684