PEX19 antibody (C-Term)

Catalog No. ABIN2788834

This anti-PEX19 antibody is a Rabbit Polyclonal antibody detecting PEX19 in WB. Suitable for Human, Mouse, Rat, Rabbit, Cow, Dog, Guinea Pig, Horse and Pig.

Quick Overview for PEX19 antibody (C-Term) (ABIN2788834)

Target: PEX19 (Peroxisomal Biogenesis Factor 19 (PEX19))

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

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX19 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-PEX19 Antibody

Binding Specificity: C-Term

Sequence: AETPTDSETT QKARFEMVLD LMQQLQDLGH PPKELAGEMP PGLNFDLDAL

Predicted Reactivity: Cow: 93%, Dog: 93%, Guinea Pig: 86%, Horse: 93%, Human: 100%, Mouse: 86%, Pig: 93%, Rabbit: 86%, Rat: 86%

Characteristics: This is a rabbit polyclonal antibody against PEX19. It was validated on Western Blot.

Purification: Affinity Purified

Application Details

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

Comment:

Antigen size: 299 AA

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: Lot specific

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 repeated 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 PEX19

Target: PEX19 (Peroxisomal Biogenesis Factor 19 (PEX19))

Alternative Name: PEX19

Background: This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. These disorders have at least 14 complementation groups, with more than one phenotype being observed for some complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS), as well as peroxisome biogenesis disorder complementation group 14 (PBD-CG14), which is also known as PBD-CGJ. Alternative splicing results in multiple transcript variants.
Alias Symbols: D1S2223E, FLJ55296, HK33, PMP1, PMPI, PXF, PXMP1
Protein Interaction Partner: FKBP7, IL23A, PEX3, UBC, PPIB, PTPLAD1, VCP, PXMP4, SLC25A17, PEX16, PEX11B, ABCD3, PMP22, EGFR, Cdkn2a, Pxmp2, TMEM54, MFSD5, PEX26, GSKIP, F11R, KIFAP3, OIP5, EIF1B, PEX11A, STK3, SRPK1, PEX14, PEX13, SMAD2, IRF3, CDC25A, NUDCD2, DSTN, NUBP2, HSPB1, PEX
Protein Size: 299

Molecular Weight: 33 kDa

Gene ID: 5824

NCBI Accession: NM_002857, NP_002848

UniProt: P40855