IMP2 Inner Mitochondrial Membrane Peptidase-Like (S. Cerevisiae) (IMMP2L) (AA 88-117), (Middle Region) antibody

Details for Product No. ABIN952890
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Antigen
Synonyms IMP2, IMP2-LIKE, AI853880
Epitope
AA 88-117, Middle Region
(7), (6), (3), (3), (1), (1)
Reactivity
Human
(17), (4), (3)
Host
Rabbit
(16), (1), (1)
Clonality
Polyclonal
Conjugate
Un-conjugated
(1), (1), (1), (1), (1), (1)
Application
Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Western Blotting (WB)
(18), (9), (9), (7), (1)
Pubmed 3 references available
Quantity 0.4 mL
Shipping to United States (Change)
Availability Will be delivered in 6 to 8 Business Days
Request Want additional data for this product?

The Independent Validation Initiative strives to provide you with high quality data. Find out more

Catalog No. ABIN952890
357.50 $
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Immunogen KLH conjugated synthetic peptide between 88~117 amino acids from the Central region of Human IMMP2L
Specificity This antibody recognizes Human IMMP2L (Center).
Purification Protein A column, followed by peptide affinity purification
Alternative Name IMMP2L
Background IMP2L complex generates mature, active proteins in the mitochondrial intermembrane space by proteolytically removing the mitochondrial targeting presequence of nuclear- encoded proteins. IMP1 (IMMP1L, MIM 612323) and IMP2 are the catalytic subunits of the IMP complex.
Alternate names: IMP2-like protein, Mitochondrial inner membrane protease subunit 2
Molecular Weight 19718 Da
Gene ID 83943
NCBI Accession NP_115938
Restrictions For Research Use only
Format Liquid
Concentration 0.25 mg/mL
Buffer PBS containing 0.09% (w/v) Sodium Azide as preservative
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 repeated freezing and thawing.
Storage 4 °C/-20 °C
Storage Comment Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer.
Expiry Date 12 months
Background publications de Krom, Staal, Ophoff et al.: "A common variant in DRD3 receptor is associated with autism spectrum disorder." in: Biological psychiatry, Vol. 65, Issue 7, pp. 625-30, 2009 (PubMed).

Trynka, Zhernakova, Romanos et al.: "Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling." in: Gut, Vol. 58, Issue 8, pp. 1078-83, 2009 (PubMed).

Need, Attix, McEvoy et al.: "A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB." in: Human molecular genetics, Vol. 18, Issue 23, pp. 4650-61, 2009 (PubMed).

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