FBXW4 Polyclonal antibody

FBXW4 Polyclonal Antibody for IHC, WB, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse

Applications

WB, IHC, ELISA

Conjugate

Unconjugated

Cat no : 10657-1-AP

Synonyms

DAC, Dactylin, FBW4, FBWD4, FBXW4, SHFM3, SHSF3



Tested Applications

Positive WB detected inmouse lung tissue, mouse liver tissue
Positive IHC detected inhuman pancreas tissue
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:200-1:1000
Immunohistochemistry (IHC)IHC : 1:50-1:500
Sample-dependent, check data in validation data gallery

Product Information

10657-1-AP targets FBXW4 in WB, IHC, ELISA applications and shows reactivity with human, mouse samples.

Tested Reactivity human, mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen FBXW4 fusion protein Ag1047 相同性解析による交差性が予測される生物種
Full Name F-box and WD repeat domain containing 4
Calculated molecular weight 46 kDa
Observed molecular weight 50 kDa
GenBank accession numberBC007380
Gene symbol FBXW4
Gene ID (NCBI) 6468
RRIDAB_2102754
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. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

Background Information

F-box proteins have been shown to be critical for the ubiquitin-mediated degradation of cellular regulatory proteins, and they are a family of eukaryotic proteins characterized by an approximately 40 amino acid motif. SCF complex, a class of ubiquitin ligases, consists of invariable components, Skp1 and Cullin, and variable components of F-box proteins, which have a primary role in determining substrate specificity. FBXW4, also known as SHFM3, encodes F-box and WD-40 domain-containing protein 4. Defects in SHFM3 are a cause of split-hand/foot malformation type 3 (SHFM3), an autosomal dominant disorder characterized by hypoplasia/aplasia of the central digits with fusion of the remaining digits.

Protocols

Product Specific Protocols
WB protocol for FBXW4 antibody 10657-1-APDownload protocol
IHC protocol for FBXW4 antibody 10657-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols