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  • KD/KO Validated

MCPH/BRIT1 Polyclonal antibody

MCPH/BRIT1 Polyclonal Antibody for WB, IHC, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse

Applications

WB, IHC, ELISA

Conjugate

Unconjugated

Cat no : 11962-1-AP

Synonyms

BRIT1, MCPH1, MCT, Microcephalin, microcephalin 1



Tested Applications

Positive WB detected inHeLa cells, L02 cells, MDA-MB-453s cells, mouse ovary tissue
Positive IHC detected inhuman prostate cancer tissue, human kidney 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 : 1:500-1:1000
Immunohistochemistry (IHC)IHC : 1:20-1:200
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

11962-1-AP targets MCPH/BRIT1 in WB, IHC, ELISA applications and shows reactivity with human, mouse samples.

Tested Reactivity human, mouse
Cited Reactivityhuman
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen MCPH/BRIT1 fusion protein Ag2567
Full Name microcephalin 1
Calculated Molecular Weight 93 kDa
Observed Molecular Weight 66 kDa, 100 kDa
GenBank Accession NumberBC030702
Gene Symbol MCPH1
Gene ID (NCBI) 79648
RRIDAB_2142989
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen 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. 20ul sizes contain 0.1% BSA.

Background Information

Primary microcdphaly refers to the clinical finding of a head circumference less than 3 standard deviations(SD) below the age- and sex-related mean, present at birth. MCPH1, the fisrt gene identified as causative for primary microcephaly, encodes a multifunctional protein that notably is linked to DNA damage checkpoint, DNA repair by homologous recombination and DNA transcription. MCPH1 is associated with premature chromosome condensation in particular. There are three mainly isoforms encoded by MCPH1 gene, full-length MCPH1 (MCPH1-FL) (~100kd), lacking the C-terminal BRCTisoform 2(~70kd) and lacking middle region isoform 3(~50kd).(PMID: 22952573 )

Protocols

Product Specific Protocols
WB protocol for MCPH/BRIT1 antibody 11962-1-APDownload protocol
IHC protocol for MCPH/BRIT1 antibody 11962-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
humanWB

FASEB J

Phosphorylation of MCPH1 isoforms during mitosis followed by isoform-specific degradation by APC/C-CDH1.

Authors - Stephanie K Meyer
  • KD Validated
humanWB, IHC

Stem Cell Res

Generation of a MCPH1 knockout human embryonic stem cell line by CRISPR/Cas9 technology.

Authors - Zerui Wang
  • KO Validated
humanWB

FEBS J

Mitotic entry upon Topo II catalytic inhibition is controlled by Chk1 and Plk1.

Authors - Maria Arroyo
  • KD Validated
humanWB

Genes (Basel)

MCPH1 Lack of Function Enhances Mitotic Cell Sensitivity Caused by Catalytic Inhibitors of Topo II.

Authors - María Arroyo
  • KD Validated

Reviews

The reviews below have been submitted by verified Proteintech customers who received an incentive forproviding their feedback.


FH

Paul (Verified Customer) (11-10-2022)

I compared several commercial antibodies for MCPH1 and this was the only one that was able to detect both isoforms in Western blotting. Importantly, these bands disappeared after treatment of cells with MCPH1 siRNA.

  • Applications: Western Blot
  • Cell Tissue Type: Human cell lines