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Thermo Fisher Scientific ALDH3B2 Monoclonal Antibody (3E6)
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Thermo Fisher Scientific ALDH3B2 Monoclonal Antibody (3E6)

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인간 ALDH3B2 단백질을 인식하는 Mouse IgG1 단일클론 항체로 ELISA에 적합합니다. GST 태그가 결합된 full-length 재조합 단백질로부터 제작되었으며, PBS(pH 7.4) 용액 형태로 제공됩니다. 연구용으로만 사용 가능하며 -20°C에서 보관합니다.

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pk
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마지막 업데이트 2025. 08. 04. 오후 10:59
Thermo Fisher Scientific H00000222-M01 ALDH3B2 Monoclonal Antibody (3E6) 100 ug pk판매 단위 pk ·
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518,100원VAT 포함 569,910원

Thermo Fisher Scientific · Thermo Fisher Scientific ALDH3B2 Monoclonal Antibody (3E6)

Applications

  • ELISA (ELISA)
    Tested Dilution: 0.3 ng/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG1, kappa
Class Monoclonal
Type Antibody
Clone 3E6
Immunogen ALDH3B2 (AAH07685, 1 a.a. ~ 385 a.a) full-length recombinant protein with GST tag (MW of GST tag alone: 26 KDa)
Conjugate Unconjugated
Form Liquid
Concentration See Label
Purification Affinity chromatography
Storage buffer PBS, pH 7.4
Contains No preservative
Storage conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping conditions Ambient (domestic); Wet ice (international)

Product Specific Information

Sequence of this protein is as follows:
MKDEPRSTNL FMKLDSVFIW KEPFGLVLII APWNYPLNLT LVLLVGALAA GSCVVLKPSE ISQGTEKVLA EVLPQYLDQS CFAVVLGGPQ ETGQLLEHKL DYIFFTGSPR VGKIVMTAAT KHLTPVTLEL GGKNPCYVDD NCDPQTVANR VAWFCYFNAG QTCVAPDYVL CSPEMQERLL PALQSTITRF YGDDPQSSPN LGRIINQKQF QRLRALLGCG RVAIGGQSNE SDRYIAPTVL VDVQETEPVM QEEIFGPILP IVNVQSVDEA IKFINWQEKP LALYAFSNSS QVVNQMLERT SSGSFGGNEG FTYISLLSVP FGGVGHSGMG RYHGKFTFDT FSHHRTCLLA PSGLEKLKEI HYPPYTDWNQ QLLRWGMGSQ SCTLL

Target Information

ALDH3B2 (aldehyde dehydrogenase 3 family, member B2), also known as ALDH8, is a 385 amino acid protein that belongs to the ALDH family and is involved in alcohol metabolism. Expressed in salivary gland tissue, ALDH3B2 catalyzes the NADP⁺-dependent conversion of aldehyde into acid.
The gene encoding ALDH3B2 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome.
Defects in genes mapped to chromosome 11 are associated with disorders such as Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema, and Smith-Lemli-Opitz syndrome.

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

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