SALL4 polyclonal antibody
* The price is valid only in USA. Please select country.
-
More Files
- More Functions
-
Specifications
Product Description
Rabbit polyclonal antibody raised against synthetic peptide of SALL4.
Immunogen
A synthetic peptide (conjugated with KLH) corresponding to C-terminus of human SALL4.
Host
Rabbit
Reactivity
Human
Form
Liquid
Purification
Protein A purification
Recommend Usage
Western Blot (1:1000)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS (0.09% sodium azide)
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
-
Applications
Western Blot (Cell lysate)
Western blot analysis of SALL4 polyclonal antibody (Cat # PAB3156) in 293 cell line lysates (35 ug/lane). SALL4 (arrow) was detected using the purified polyclonal antibody. -
Gene Info — SALL4
Entrez GeneID
57167Protein Accession#
NP_065169;Q9UJQ4Gene Name
SALL4
Gene Alias
DRRS, HSAL4, MGC133050, ZNF797, dJ1112F19.1
Gene Description
sal-like 4 (Drosophila)
Gene Ontology
HyperlinkGene Summary
The protein encoded by this gene may be a zinc finger transcription factor. Defects in this gene are a cause of Duane-radial ray syndrome (DRRS). [provided by RefSeq
Other Designations
OTTHUMP00000031296|sal-like 4
-
Interactomes
-
Diseases
-
Publication Reference
-
Multigene deletions on chromosome 20q13.13-q13.2 including SALL4 result in an expanded phenotype of Okihiro syndrome plus developmental delay.
Borozdin W, Graham JM Jr, Bohm D, Bamshad MJ, Spranger S, Burke L, Leipoldt M, Kohlhase J.
Human Mutation 2007 Aug; 28(8):830.
-
Bmi-1 is a target gene for SALL4 in hematopoietic and leukemic cells.
Yang J, Chai L, Liu F, Fink LM, Lin P, Silberstein LE, Amin HM, Ward DC, Ma Y.
PNAS 2007 Jun; 104(25):10494.
Application:ChIP, Human, HEK 293 cells.
-
IVIC syndrome is caused by a c.2607delA mutation in the SALL4 locus.
Paradisi I, Arias S.
American Journal of Medical Genetics. Part A 2007 Feb; 143(4):326.
-
Multigene deletions on chromosome 20q13.13-q13.2 including SALL4 result in an expanded phenotype of Okihiro syndrome plus developmental delay.
- +1-909-264-1399
+1-909-992-0619
Toll Free : +1-877-853-6098 - +1-909-992-3401
- sales@abnova.com