SMCR7 anticorps (N-Term)

N° du produit ABIN2791915

Cet anticorps anti-SMCR7 est un anticorps Lapin Polyclonal détectant SMCR7 dans WB. Adapté pour Humain, Cobaye, Cheval et Rat.

Aperçu rapide pour SMCR7 anticorps (N-Term) (ABIN2791915)

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

Reactivité: Humain, Cobaye, Cheval, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SMCR7 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-SMCR7 anticorps

Épitope: N-Term

Séquence: FSQKRGKRRS DEGLGSMVDF LLANARLVLG VGGAAVLGIA TLAVKRFIDR

Homologie: Guinea Pig: 79%, Horse: 86%, Human: 100%, Rat: 79%

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

Purification: Affinity Purified

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

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

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.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Conseil sur la manipulation: Avoid repeat freeze-thaw cycles.

Stock: -20 °C

Stockage commentaire: 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.

Détails sur SMCR7

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

Autre désignation: SMCR7

Sujet: 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

Poids moléculaire: 50 kDa

ID gène: 125170

NCBI Accession: NM_148886, NP_683684