Thermo Fisher Scientific C10orf32 Polyclonal Antibody

Applications

Tested Dilution

Publications

Immunohistochemistry (Paraffin) (IHC (P))

1:500-1:1,000

-

Immunocytochemistry (ICC/IF)

0.25-2 µg/mL

-

Product Specifications

Species Reactivity

Human

Host/Isotype

Rabbit / IgG

Class

Polyclonal

Type

Antibody

Immunogen

Recombinant protein corresponding to Human C10orf32. Recombinant protein control fragment (Product #RP-97173). if (typeof window.$mangular === undefined || !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{targetFamily:C10orf32,uniProtId:Q96B45-1,ncbiNodeId:9606,antigenRange:13-106,antigenLength:106,antigenImageFileName:PA5-58040_C10orf32_Q96B45-1_Rabbit.svg,antigenImageFileNamePDP:PA5-58040_C10orf32_Q96B45-1_Rabbit_PDP.jpeg,sortOrder:1}\]; $mangular.isB2BCMGT = false; $mangular.isEpitopesModalImageMultiSizeEnabled = true;

View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

0.4 mg/mL

Purification

Antigen affinity chromatography

Storage buffer

PBS, pH 7.2, with 40% glycerol

Contains

0.02% sodium azide

Storage conditions

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

Shipping conditions

Wet ice

RRID

AB_2638664

Product Specific Information

Immunogen sequence: FGQSVKGLLT EKVTTCGTDV IALTKQVLKG SRSSELLGQA ARNMVLQEDA ILHSEDSLRK MAIITTHLQY QQEAIQKNVE QSSDLQDQLN HLLK

Highest antigen sequence identity to the following orthologs: Mouse - 97%, Rat - 97%.

Target Information

C10orf32 (chromosome 10 open reading frame 32) is a 105 amino acid protein that belongs to the UPF0693 family. The gene encoding C10orf32 maps to human chromosome 10, which spans nearly 135 million base pairs, makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie-Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman`s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.