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Thermo Fisher Scientific HCCS Polyclonal Antibody
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Thermo Fisher Scientific HCCS Polyclonal Antibody

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HCCS 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody. Western blot, IHC, ICC/IF에 적합하며 Human, Mouse, Rat에 반응. 항원 친화 크로마토그래피로 정제되어 높은 특이성과 재현성을 제공.

카탈로그번호
PA551783
판매단위
pk
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마지막 업데이트 2025. 08. 03. 오후 11:24
Thermo Fisher Scientific PA551783 HCCS Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific HCCS Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution References
Western Blot (WB) 0.04–0.4 µg/mL -
Immunohistochemistry (Paraffin) (IHC (P)) 1:20–1:50 -
Immunocytochemistry (ICC/IF) 0.25–2 µg/mL -

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human HCCS. Recombinant protein control fragment (Product #RP-92157)
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_2642331

Product Specific Information

Immunogen sequence:
YVECPIRGTA AENKENLDPS NLMPPPNQTP APDQPFALST VREESSIPRA DSEKKWVYPS EQMFWNAMLK KGWKWKDEDI SQKDMYNIIR IHNQNNEQAW KEILKWEALH AAECPCGPSL IRFGGKAKEY SPRARIRSWM GYEL

Highest antigen sequence identity to the following orthologs:

  • Mouse: 90%
  • Rat: 92%

Target Information

CCHL (cytochrome c-type heme lyase), also known as HCCS (holocytochrome c-type synthase), is a 268 amino acid mitochondrial inner membrane protein belonging to the cytochrome c-type heme lyase family.
It contains two HRM (heme regulatory motif) repeats and is involved in the covalent linkage of a heme group to an apoprotein of cytochrome c.
The gene encoding HCCS is located on the human X chromosome.
Mutations in this gene cause microphthalmia syndromic type 7 (MCOPS7), also known as MIDAS syndrome or microphthalmia with linear skin defects (MLS), an X-linked male-lethal disorder resulting in eye deformation, microphthalmia, and linear skin defects in affected females.


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

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