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Thermo Fisher Scientific NSD2 Monoclonal Antibody (CL1057)
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Thermo Fisher Scientific NSD2 Monoclonal Antibody (CL1057)

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Human NSD2 단백질을 인식하는 Mouse IgG1 단클론 항체로, IHC(P) 및 ICC/IF 실험에 적합합니다. 단백질 A로 정제된 액상 형태이며, 4°C 단기 보관 및 -20°C 장기 보관이 가능합니다. 연구용으로만 사용됩니다.

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마지막 업데이트 2025. 08. 05. 오후 08:03
Thermo Fisher Scientific MA524620 NSD2 Monoclonal Antibody (CL1057) 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific NSD2 Monoclonal Antibody (CL1057)

Applications

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: 1:200–1:500

Immunocytochemistry (ICC/IF)

  • Tested Dilution: 2–10 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone CL1057
Immunogen Recombinant protein corresponding to Human NSD2
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A
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_2637235

Product Specific Information

Immunogen sequence:
SANGKTPSCE VNRECSVFLS KAQLSSSLQE GVMQKFNGHD ALPFIPADKL KDLTSRVFNG EPGAHDAKLR FESQEMKGIG TPPNTTPIKN GSPEIKLKIT KTYMNGKPLF ESSICGD

  • Highest antigen sequence identity to the following orthologs: Mouse – 91%, Rat – 91%
  • Binds to an epitope located within the peptide sequence RVFNGEPGAHDAKLR as determined by overlapping synthetic peptides.

Target Information

This gene encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene maps to the 165 kb WHS critical region and has also been involved in the chromosomal translocation t(4;14)(p16.3;q32.3) in multiple myelomas. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. Some transcript variants are nonsense-mediated mRNA (NMD) decay candidates, hence not represented as reference sequences.


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

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