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Thermo Fisher Scientific BRP44L Polyclonal Antibody
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Thermo Fisher Scientific BRP44L Polyclonal Antibody

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BRP44L 단백질을 인식하는 Rabbit Polyclonal 항체로, Western blot, IHC, ICC/IF에 적합. 항원 친화 크로마토그래피로 정제되었으며, PBS(40% glycerol) 버퍼에 보관. 인간 BRP44L 재조합 단백질로 면역화되어 높은 특이성과 재현성을 제공.

카탈로그번호
PA560929
판매단위
pk
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마지막 업데이트 2025. 08. 01. 오후 01:43
Thermo Fisher Scientific PA560929 BRP44L Polyclonal Antibody 100 ul pk판매 단위 pk ·
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799,600원VAT 포함 879,560원

Thermo Fisher Scientific · Thermo Fisher Scientific BRP44L Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 0.04–0.4 µg/mL
Immunohistochemistry (Paraffin) (IHC-P) 1:500–1:1,000
Immunocytochemistry (ICC/IF) 0.25–2 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human BRP44L (Recombinant protein control fragment: Product #RP-100810)
Conjugate Unconjugated
Form Liquid
Concentration 0.1 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_2638597

Product Specific Information

Immunogen sequence:
MAGALVRKAA DYVRSKDFRD YLMSTHFWGP VANWGLPIAA INDMKKSPEI ISGR

Highest antigen sequence identity to the following orthologs:

  • Mouse – 100%
  • Rat – 100%

Target Information

BRP44L (Brain Protein 44-like protein), also known as HSPC040 or CGI-129, is a 109 amino acid mitochondrial protein belonging to the UPF0041 family.
The BRP44L gene maps to human chromosome 6, which contains around 1,200 genes within 170 million base pairs of sequence (~6% of the human genome).

Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer, suggesting the presence of a cancer susceptibility locus.
Chromosome 6 is also linked to several genetic conditions including:

  • Porphyria cutanea tarda (via HFE gene mutations)
  • Parkinson’s disease (via PARK2 gene)
  • Rheumatic diseases (via MHC complex)
  • Stickler syndrome, 21-hydroxylase deficiency, and maple syrup urine disease
  • A bipolar disorder susceptibility locus on the q arm

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

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