SMCR7 antibody (N-Term)

Catalog No. ABIN2774579

This Rabbit Polyclonal antibody specifically detects SMCR7 in WB. It exhibits reactivity toward Mouse, Human, Guinea Pig, Horse, Rat, Cow, Dog and Rabbit.

Quick Overview for SMCR7 antibody (N-Term) (ABIN2774579)

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

Reactivity: Mouse, Human, Guinea Pig, Horse, Rat, Cow, Dog, Rabbit

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: IDRATSPRDE DDTKADSWKE LSLLKATPHL QPRPPPAALS QPVLPLAPSS

Predicted Reactivity: Cow: 92%, Dog: 85%, Guinea Pig: 79%, Horse: 77%, Human: 100%, Mouse: 86%, Rabbit: 77%, Rat: 86%

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.
Protein Interaction Partner: AGTRAP, UBQLN1, RABAC1, DNM1L, UBC, UBQLN4, PSMF1,
Protein Size: 205

Molecular Weight: 22 kDa

Gene ID: 125170