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Alpha Parvin/Actopaxin Polyclonal antibody

Alpha Parvin/Actopaxin Polyclonal Antibody for IF, WB,ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat, Canine

Applications

WB, IF, CoIP,ELISA

Conjugate

Unconjugated

Cat no : 55268-1-AP

Synonyms

Actopaxin, Alpha parvin, CH ILKBP, MXRA2, PARVA, parvin, alpha, α-Parvin



Tested Applications

Positive WB detected inU2OS cells, HeLa cells, mouse kidney tissue
Positive IF detected inMDCK cells

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:200-1:1000
Immunofluorescence (IF)IF : 1:10-1:100
Sample-dependent, check data in validation data gallery

Product Information

55268-1-AP targets Alpha Parvin/Actopaxin in WB, IF, CoIP,ELISA applications and shows reactivity with human, mouse, rat, Canine samples.

Tested Reactivity human, mouse, rat, Canine
Cited Reactivitymouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Peptide
Full Name parvin, alpha
Calculated molecular weight 42 kDa
Observed molecular weight 45-50 kDa
GenBank accession numberNM_018222
Gene symbol PARVA
Gene ID (NCBI) 55742
Conjugate Unconjugated
Form Liquid
Purification Method Antigen affinity purification
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore at -20°C. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.

Background Information

α-Parvin (PARVA), also named as MXRA2, Actopaxin and CH-ILKBP, belongs to the parvin family. It probably plays a role in the regulation of cell adhesion and cytoskeleton organization. (PMID:11134073) This antibody is specific to α-Parvin.

Protocols

Product Specific Protocols
WB protocol for Alpha Parvin/Actopaxin antibody 55268-1-APDownload protocol
IHC protocol for Alpha Parvin/Actopaxin antibody 55268-1-APDownload protocol
IF protocol for Alpha Parvin/Actopaxin antibody 55268-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
mouseWB,CoIP

Proteome Sci

Label-free quantitative mass spectrometry analysis of differential protein expression in the developing cochlear sensory epithelium.

Authors - Lancia N F Darville