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MABC576

Anti-HOIL-1 Antibody, clone 2E2

clone 2E2, from mouse

Synonym(s):

RanBP-type and C3HC4-type zinc finger-containing protein 1, HBV-associated factor 4, Heme-oxidized IRP2 ubiquitin ligase 1, HOIL-1, Hepatitis B virus X-associated protein 4, RING finger protein 54, Ubiquitin-conjugating enzyme 7-interacting protein 3, HO

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About This Item

UNSPSC Code:
12352203
NACRES:
NA.43
eCl@ss:
32160702
Conjugate:
unconjugated
Clone:
2E2, monoclonal
Application:
ICC, WB
Citations:
13
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biological source

mouse

Quality Level

conjugate

unconjugated

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

2E2, monoclonal

species reactivity

mouse, human

technique(s)

immunocytochemistry: suitable, western blot: suitable

isotype

IgG1κ

NCBI accession no.

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Gene Information

human ... RBCK1(10616)

General description

RanBP-type and C3HC4-type zinc finger-containing protein 1 (UniProt Q9BYM8; also known as HOIL-1, HBV-associated factor 4, Heme-oxidized IRP2 ubiquitin ligase 1, Hepatitis B virus X-associated protein 4, RBCC protein interacting with PKC1, RING finger protein 54, Ubiquitin-conjugating enzyme 7-interacting protein 3) is encoded by the RBCK1 gene (also known as C20orf18, HOIL1, PBMEI, RBCK2, RNF54, UBCE7IP3, XAP3, XAP4, ZRANB4) (Gene ID 10616) in human. The linear ubiquitin assembly complex (LUBAC) is comprised of two RING-IBR-RING (RBR)-containing E3 ligases, HOIL-1L and HOIP. LUBAC conjugates a head-to-tail-linked linear polyubiquitin chain onto lysine residues on substrate proteins. Ovarian tumor deubiquitinating enzyme (DUB) with linear linkage specificity (OTULIN/Gumby/FAM105B) and cylindromatosis (CYLD) are two DUBs that catalyze the cleavage linear polyubiquitin chains. OTULIN and CYLD interact with the N-terminal PNGase/UBA or UBX (PUB) domain of HOIP and negatively regulate LUBAC-mediated cellular processes. LUBAC is reported to suppress IFN-dependent antiviral activity by mediating TRIM25 degradation and competing against TRIM25 for RIG-I interaction.
~57 kDa observed

Immunogen

Epitope: Near C-terminus
GST-tagged recombinant protein corresponding to human HOIL-1 near the C-terminus.

Application

Research Category
Apoptosis & Cancer
Research Sub Category
Apoptosis - Additional
This Anti-HOIL-1 Antibody, clone 2E2 is validated for use in Western Blotting, Immunocytochemistry for the detection of HOIL-1 .
Western Blotting Analysis: A representative lot detected HOIL-1 in HeLa, SH-SY5Y, and U20S cells (Kirisako, T., et al (2006). EMBO J. 25(20):48877-4887).
Western Blotting Analysis: A representative lot detected HOIL-1 in mouse liver extracts (Tokunaga, F., et al (2009). Nat. Cell Biol. 11(2):123-132).
Western Blotting Analysis: A representative lot detected HOIL-1 in MEFs (Takiuchi, T., et al (2014). Genes Cells. 19(3):254-272).
Immunocytochemistry Analysis: A representative lot detected HOIL-1 in HeLa cells with or without Sendai virus (SeV) infection (Inn, K.S., et al. (2011). Mol Cell. 41(3):354-365).

Biochem/physiol Actions

Clone 2E2 reacts with isoform 1 (HOIL-1L) and isoform 2, but not isoform 3.

Physical form

Format: Purified
Protein G Purified
Purified mouse monoclonal IgG1κ antibody in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Preparation Note

Stable for 1 year at 2-8°C from date of receipt.

Analysis Note

Evaluated by Western Blotting in THP-1 cell lysate.

Western Blotting Analysis: 2.0 µg/mL of this antibody detected HOIL-1 in 10 µg of THP-1 cell lysate.

Other Notes

Concentration: Please refer to lot specific datasheet.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.


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Storage Class

12 - Non Combustible Liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable



Certificates of Analysis (COA)

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Related Content

A major focus of breast cancer research is to understand the mechanisms responsible for disease progression and drug resistance. Toward that end, it has been found that approximately two thirds of all human breast carcinomas overexpress the Estrogen Receptor α (ERα) protein and it remains the primary pharmacological target for endocrine therapy1,2. The normal cellular function of ERα is as a transcription factor that mediates a wide variety of physiological processes, many of which are dependent upon phosphorylation of the receptor at specific amino acid residues3,4. Indeed, ERα is known to be phosphorylated at a multitude of different sites, yet how these all correlate to disease remains unclear5. Here, we interrogated multiple sites of ERα for phosphorylation status by screening an extensive panel of different breast cancer patient samples and other non-breast cancer tissue microarray (TMA) slide samples to determine their relevance to disease.


Hirotsugu Oda et al.
Frontiers in immunology, 10, 479-479 (2019-04-03)
Background: HOIP is the catalytic subunit of the linear ubiquitination chain assembly complex (LUBAC) that is essential for NF-κB signaling and thus proper innate and adaptive immunity. To date only one patient with HOIP deficiency has been reported with clinical
A ubiquitin ligase complex assembles linear polyubiquitin chains.
Kirisako, T; Kamei, K; Murata, S; Kato, M; Fukumoto, H; Kanie, M; Sano, S; Tokunaga et al.
The Embo Journal null
Involvement of linear polyubiquitylation of NEMO in NF-kappaB activation.
Tokunaga, F; Sakata, S; Saeki, Y; Satomi, Y; Kirisako, T; Kamei, K; Nakagawa, T; Kato et al.
Nature Cell Biology null



Global Trade Item Number

SKUGTIN
MABC57604055977173703