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AB176277

Anti-SARM antibody

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(1 Publication)

Rabbit Polyclonal SARM antibody. Suitable for WB and reacts with Human samples. Cited in 1 publication. Immunogen corresponding to Synthetic Peptide within Human SARM1.

View Alternative Names

KIAA0524, SAMD2, SARM, SARM1, NAD(+) hydrolase SARM1, NADase SARM1, hSARM1, NADP(+) hydrolase SARM1, Sterile alpha and Armadillo repeat protein, Sterile alpha and TIR motif-containing protein 1, Sterile alpha motif domain-containing protein 2, Tir-1 homolog, MyD88-5, SAM domain-containing protein 2, HsTIR

1 Images
Western blot - Anti-SARM antibody (AB176277)
  • WB

Supplier Data

Western blot - Anti-SARM antibody (AB176277)

Lane 1:

Western blot - Anti-SARM antibody (ab176277) at 1 µg/mL

Lane 2:

Western blot - Anti-SARM antibody (ab176277) at 2 µg/mL

All lanes:

Human kidney tissue lysate at 15 µg

Predicted band size: 79 kDa

true

Key facts

Host species

Rabbit

Clonality

Polyclonal

Isotype

IgG

Carrier free

No

Reacts with

Human

Applications

WB

applications

Immunogen

Synthetic Peptide within Human SARM1. The exact immunogen used to generate this antibody is proprietary information.

Q6SZW1

Specificity

At least three alternatively spliced transcript variants encoding distinct isoforms have been observed. ab176277 recognizes the longest isoform.

Reactivity data

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Properties and storage information

Form
Liquid
Purification technique
Affinity purification Immunogen
Storage buffer
pH: 7.2 Preservative: 0.02% Sodium azide Constituents: PBS
Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1-2 weeks
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

The sterile alpha and HEAT/Armadillo motif-containing protein commonly known as SARM is a member of the death domain superfamily. It has a molecular mass of approximately 68 kDa. SARM is expressed in the nervous system and various immune cells. Mechanically SARM functions as an adaptor protein involved in signaling pathways related to immunity and neuroprotection. It primarily modulates signaling cascades by interacting with other key proteins within the cellular environment.
Biological function summary

SARM engages in processes that are important to maintaining neurological health and regulating immune responses. It serves as a part of the innate immunity complex where it contributes to the regulation of inflammatory responses. SARM can also influence mitochondrial function indicating it plays a significant role in cellular energy management and apoptosis control. These multifaceted functions highlight its engagement in complex and dynamic cellular processes.

Pathways

SARM plays an important role in the toll-like receptor (TLR) signaling pathway and mitochondrial apoptosis pathway. SARM interacts closely with TLRs to modulate immune responses particularly impacting the production of type I interferons. In the mitochondrial apoptosis pathway SARM relates to proteins like TRAF6 impacting cell death and survival. Its involvement in these pathways reflects its essential function in controlling cellular stress responses.

SARM has been implicated in neurological diseases such as Alzheimer's disease and infectious diseases such as viral encephalitis. In Alzheimer's disease SARM interacts with other proteins like amyloid precursor protein (APP) modulating pathways that may exacerbate neurodegeneration. In viral encephalitis SARM mediates immune responses providing a link to immune-related proteins like MyD88 which contribute to neuronal damage during infection. This makes SARM a target of interest for therapeutic interventions in both neurological and infectious diseases.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

NAD(+) hydrolase, which plays a key role in axonal degeneration following injury by regulating NAD(+) metabolism (PubMed : 25908823, PubMed : 27671644, PubMed : 28334607). Acts as a negative regulator of MYD88- and TRIF-dependent toll-like receptor signaling pathway by promoting Wallerian degeneration, an injury-induced form of programmed subcellular death which involves degeneration of an axon distal to the injury site (PubMed : 15123841, PubMed : 16964262, PubMed : 20306472, PubMed : 25908823). Wallerian degeneration is triggered by NAD(+) depletion : in response to injury, SARM1 is activated and catalyzes cleavage of NAD(+) into ADP-D-ribose (ADPR), cyclic ADPR (cADPR) and nicotinamide; NAD(+) cleavage promoting cytoskeletal degradation and axon destruction (PubMed : 25908823, PubMed : 28334607, PubMed : 30333228, PubMed : 31128467, PubMed : 31439792, PubMed : 31439793, PubMed : 32049506, PubMed : 32828421, PubMed : 33053563). Also able to hydrolyze NADP(+), but not other NAD(+)-related molecules (PubMed : 29395922). Can activate neuronal cell death in response to stress (PubMed : 20306472). Regulates dendritic arborization through the MAPK4-JNK pathway (By similarity). Involved in innate immune response : inhibits both TICAM1/TRIF- and MYD88-dependent activation of JUN/AP-1, TRIF-dependent activation of NF-kappa-B and IRF3, and the phosphorylation of MAPK14/p38 (PubMed : 16964262).
See full target information SARM1

Publications (1)

Recent publications for all applications. Explore the full list and refine your search

Nutrition & metabolism 19:17 PubMed35248109

2022

The combination of endurance exercise and SGTC (Salvia-Ginseng-Trigonella-Cinnamon) ameliorate mitochondrial markers' overexpression with sufficient ATP production in the skeletal muscle of mice fed AGEs-rich high-fat diet.

Applications

Unspecified application

Species

Unspecified reactive species

Maryam Haghparast Azad,Iman Niktab,Shaghayegh Dastjerdi,Navid Abedpoor,Golbarg Rahimi,Zahra Safaeinejad,Maryam Peymani,Farzad Seyed Forootan,Majid Asadi-Shekaari,Mohammad Hossein Nasr Esfahani,Kamran Ghaedi
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